Secondary battery and method for using secondary battery

ABSTRACT

A secondary battery of the present invention includes at least a positive electrode, a negative electrode, a separation layer that spatially separates the positive electrode and the negative electrode, and an ion conductor that is held between the positive electrode and the negative electrode and has a function of conducting ions between the positive electrode and the negative electrode. In addition, in an initial stage of using the secondary battery, the secondary battery has a characteristic of a potential increase rate of the positive electrode immediately before completion of full charging being smaller than a potential decrease rate of the negative electrode immediately before the completion of full charging and a characteristic of a potential decrease rate of the positive electrode immediately before completion of full discharging being smaller than a potential increase rate of the negative electrode immediately before the completion of full discharging.

TECHNICAL FIELD

The present invention relates to a secondary battery and a method forusing a secondary battery.

BACKGROUND ART

As a technique regarding the extension of the service lives of secondarybatteries such as lithium ion secondary batteries, for example, atechnique described in Patent Document 1 is exemplified.

Patent Document 1 describes a method for charging and discharging alithium secondary battery including a positive electrode having apositive electrode active material capable of storing and discharginglithium ions, a negative electrode having a negative electrode activematerial capable of storing and discharging lithium ions, a separatordisposed between the positive electrode and the negative electrode, andan electrolyte having a lithium ion conduction property, in which thepositive electrode active material includes a lithium-containingtransition metal oxide, a reversible capacity of the negative electrodeis greater than an available capacity of the positive electrode, andfirst charging and discharging in which discharging is ended bydischarging the charged positive electrode until a first potential VDp1that is smaller than 2.7 V with reference to lithium metal is reached iscarried out.

RELATED DOCUMENT Patent Document

[Patent Document 1] Japanese Patent No. 5117638

SUMMARY OF THE INVENTION Technical Problem

In the method of Patent Document 1, it is necessary to control thepotential of the positive electrode during discharging to reach a valuethat is lower than 2.7 V (Li⁺/Li). The positive electrode and thenegative electrode deteriorate separately depending on environmentsunder which the electrodes are used, and thus the relationship between apositive electrode potential and a negative electrode potential changesin association with the deterioration. Therefore, the positive electrodepotential cannot be estimated from a potential between the positiveelectrode and the negative electrode, and there is a problem in that aprocedure of accurately evaluating the positive electrode potentialbecomes necessary. In addition, when the deterioration increases thepotential of the negative electrode up to approximately 2.7 V (Li⁺/Li)before the potential of the positive electrode becomes lower than 2.7 V(Li⁺/Li) during discharging, and thus the potential between the positiveelectrode and the negative electrode becomes near zero voltage, apossibility of an incapability of setting the potential of the positiveelectrode to be lower than 2.7 V (Li⁺/Li) can be considered. In thiscase, there is another problem in that it becomes impossible to use thepositive electrode and the negative electrode as a battery even when acapacity large enough to operate the electrodes remains.

The present invention has been made in consideration of theabove-described circumstance and provides a secondary battery having along product service life and a method for using a secondary batterycapable of extending the product service life.

Solution to Problem

The present inventors repeated intensive studies in order to achieve theabove-described object. As a result, the present inventors found that,when the charging and discharging characteristics of a positiveelectrode and a negative electrode in an initial stage of using asecondary battery are set in a specific relationship, it is possible toextend the product service life of the secondary battery and completedthe present invention.

That is, according to the present invention, there is provided asecondary battery including at least a positive electrode, a negativeelectrode, a separation layer that spatially separates the positiveelectrode and the negative electrode, and an ion conductor that is heldbetween the positive electrode and the negative electrode and has afunction of conducting ions between the positive electrode and thenegative electrode,

in which, in an initial stage of using the secondary battery, thesecondary battery has

a characteristic of a potential increase rate of the positive electrodeimmediately before completion of full charging being smaller than apotential decrease rate of the negative electrode immediately before thecompletion of full charging and

a characteristic of a potential decrease rate of the positive electrodeimmediately before completion of full discharging being smaller than apotential increase rate of the negative electrode immediately before thecompletion of full discharging.

In addition, according to the present invention,

there is provided a method for using a secondary battery including atleast a positive electrode, a negative electrode, a separation layerthat spatially separates the positive electrode and the negativeelectrode, and an ion conductor that is held between the positiveelectrode and the negative electrode and has a function of conductingions between the positive electrode and the negative electrode,

in which, in an initial stage of using the secondary battery, thesecondary battery is used under a condition of a potential increase rateof the positive electrode immediately before completion of full chargingbeing smaller than a potential decrease rate of the negative electrodeimmediately before the completion of full charging and is used under acondition of a potential decrease rate of the positive electrodeimmediately before completion of full discharging being smaller than apotential increase rate of the negative electrode immediately before thecompletion of full discharging.

Advantageous Effects of Invention

According to the present invention, it is possible to provide asecondary battery having a long product service life and a method forusing a secondary battery capable of extending the product service life.

BRIEF DESCRIPTION OF THE DRAWINGS

The above-described object and other objects, characteristics, andadvantages will be further clarified using a preferred embodimentdescribed below and the accompanying drawings below.

FIG. 1 is a cross-sectional view showing an example of a structure of asecondary battery of an embodiment according to the present invention.

FIG. 2 is views showing examples of relationships between charge anddischarge characteristics of a positive electrode and charge anddischarge characteristics of a negative electrode in the secondarybattery of the embodiment of the present invention, FIG. 2(a) shows anexample of the relationship between the charge and dischargecharacteristics of the positive electrode and the charge and dischargecharacteristics of the negative electrode in an initial stage of usingthe secondary battery, and FIG. 2(b) shows an example of therelationship between the charge and discharge characteristics of thepositive electrode and the charge and discharge characteristics of thenegative electrode in a late stage of using the secondary battery.

FIG. 3 is a view showing an example of a relationship between first-timecharge and discharge characteristics of the positive electrode andfirst-time charge and discharge characteristics of the negativeelectrode in the case of using an electrode element in which thepositive electrode has a larger irreversible capacity than the negativeelectrode.

FIG. 4 is a schematic view for describing correction of the relationshipbetween the first-time charge and discharge characteristics of thepositive electrode and the first-time charge and dischargecharacteristics of the negative electrode in Example 1.

FIG. 5 is a schematic view for describing the correction of therelationship between the first-time charge and discharge characteristicsof the positive electrode and the first-time charge and dischargecharacteristics of the negative electrode in Example 2.

FIG. 6 is a view showing an example of the relationship between thefirst-time charge and discharge characteristics of the positiveelectrode and the first-time charge and discharge characteristics of thenegative electrode in the case of using an electrode element in whichthe negative electrode has a larger irreversible capacity than thepositive electrode.

FIG. 7 is a schematic view for describing the correction of therelationship between the first-time charge and discharge characteristicsof the positive electrode and the first-time charge and dischargecharacteristics of the negative electrode in Example 3.

FIG. 8 is a schematic view for describing the correction of therelationship between the first-time charge and discharge characteristicsof the positive electrode and the first-time charge and dischargecharacteristics of the negative electrode in Example 4.

DESCRIPTION OF EMBODIMENTS

Hereinafter, an embodiment of the present invention will be describedusing drawings. In all of the drawings, the same constituent elementwill be given the same reference sign and will not be repeated. Inaddition, individual constituent elements in the drawings show shapes,sizes, and disposition relationships schematically enough to understandthe present invention, and thus the shapes, the sizes, and thedisposition relationships do not match actual ones. In addition, in thepresent embodiment, unless particularly otherwise described, numericalranges “A to B” indicate equal to and more than A and equal to and lessthan B.

<Secondary Battery and Method for Using Secondary Battery>

Hereinafter, a secondary battery 10 according to the present embodimentand a method for using the secondary battery 10 will be described. FIG.1 is a cross-sectional view showing an example of a structure of thesecondary battery 10 of an embodiment according to the presentinvention. FIG. 2 is views showing examples of relationships betweencharge and discharge characteristics of a positive electrode 11 andcharge and discharge characteristics of a negative electrode 12 in thesecondary battery 10 of the embodiment of the present invention, FIG.2(a) shows an example of the relationship between the charge anddischarge characteristics of the positive electrode 11 and the chargeand discharge characteristics of the negative electrode 12 in an initialstage of using the secondary battery 10, and FIG. 2(b) shows an exampleof the relationship between the charge and discharge characteristics ofthe positive electrode 11 and the charge and discharge characteristicsof the negative electrode 12 in a late stage of using the secondarybattery 10.

As shown in FIG. 1, the secondary battery 10 according to the presentembodiment includes at least the positive electrode 11, the negativeelectrode 12, a separation layer 5 that spatially separates the positiveelectrode 11 and the negative electrode 12, and an ion conductor that isheld between the positive electrode 11 and the negative electrode 12 andhas a function of conducting ions between the positive electrode 11 andthe negative electrode 12. In addition, in an initial stage of using thesecondary battery 10, the secondary battery has a characteristic of apotential increase rate of the positive electrode 11 immediately beforethe completion of full charging being smaller than a potential decreaserate of the negative electrode 12 immediately before the completion offull charging and a characteristic of a potential decrease rate of thepositive electrode 11 immediately before the completion of fulldischarging being smaller than a potential increase rate of the negativeelectrode 12 immediately before the completion of full discharging.

That is, in the initial stage of using the secondary battery 10, thesecondary battery is used under a condition of the potential increaserate of the positive electrode 11 immediately before the completion offull charging being smaller than the potential decrease rate of thenegative electrode 12 immediately before the completion of full chargingand is used under a condition of the potential decrease rate of thepositive electrode 11 immediately before the completion of fulldischarging being smaller than the potential increase rate of thenegative electrode 12 immediately before the completion of fulldischarging.

Here, in the present embodiment, the completion of full dischargingrefers to a state in which the voltage of the battery reaches a voltageset as a discharge end voltage, and the completion of full chargingrefers to a state in which the voltage of the battery reaches a voltageset as a charge end voltage. Meanwhile, the discharge end voltage andthe charge end voltage are set by a combination of the positiveelectrode and the negative electrode and can be determined on the basisof well-known information.

In addition, in the present embodiment, in the later state of usingrefers to, in a period of time of the secondary battery 10 being used, apoint in a time at which some of conduction ions that contribute tocharging and discharging decrease due to the absorption into a reactionproduct by the decomposition of an electrolytic solution or the like, anavailable portion in the capacity of the positive electrode 11 shifts,and the potential increase rate of the positive electrode 11 immediatelybefore the completion of full charging becomes larger than the potentialdecrease rate of the negative electrode 12 immediately before thecompletion of full charging.

The positive electrode 11 has a positive electrode current collector 3constituted of a metal foil such as an aluminium foil or the like and apositive electrode active material layer 1 containing a positiveelectrode active material provided on one surface of the positiveelectrode current collector 3.

The negative electrode 12 has a negative electrode current collector 4constituted of a metal foil such as a copper foil or the like and anegative electrode active material layer 2 containing a negativeelectrode active material provided on one surface of the negativeelectrode current collector 4.

The positive electrode 11 and the negative electrode 12 are laminatedtogether through the separation layer 5 so that the positive electrodeactive material layer 1 and the negative electrode active material layer2 face each other. As the separation layer 5, for example, a separatorconstituted of a microporous film made of a non-woven fabric or apolyolefin (polypropylene, polyethylene, or the like) can be used.

An electrode element constituted of the positive electrode 11, theseparation layer 5, and the negative electrode 12 are stored in, forexample, a container constituted of exterior bodies 6 and 7. As theexterior bodies 6 and 7, an aluminium laminate film can be used.

A positive electrode tab 9 is connected to the positive electrodecurrent collector 3, a negative electrode tab 8 is connected to thenegative electrode current collector 4, and these tabs are extractedoutside the container. An ion conductor is injected and sealed in thecontainer. It is also possible to form a structure in which an electrodegroup obtained by laminating a plurality of electrode elements is storedin the container.

Next, a relationship of the charge and discharge characteristics betweenthe positive electrode 11 and the negative electrode 12 of the secondarybattery 10 according to the present embodiment will be described.

First, in the secondary battery 10 according to the present embodiment,as shown in FIG. 2(a), in the initial stage of using the secondarybattery 10, the potential of the positive electrode 11 tends to increaseand the potential of the negative electrode 12 tends to decreaseimmediately before the completion of full charging.

In addition, the secondary battery 10 according to the presentembodiment, as shown in FIG. 2(a), has a characteristic that thepotential increase rate of the positive electrode 11 immediately beforethe completion of full charging is smaller than the potential decreaserate of the negative electrode 12 immediately before the completion offull charging in the initial stage of using the secondary battery 10.That is, the secondary battery 10 according to the present embodimentis, as shown in FIG. 2(a), used under a condition of the potentialincrease rate of the positive electrode 11 immediately before thecompletion of full charging being smaller than the potential decreaserate of the negative electrode 12 immediately before the completion offull charging in the initial stage of using the secondary battery 10.

In addition, the secondary battery 10 according to the presentembodiment is constituted so that, in the initial stage of using thesecondary battery 10, the absolute value of the potential increase rateper capacity or per time of the positive electrode 11 immediately beforethe completion of full charging becomes smaller than the potentialdecrease rate of the negative electrode 12 immediately before thecompletion of full charging.

That is, in the initial stage of using the secondary battery 10, the endof charging is mainly determined by a decrease in the potential of thenegative electrode 12.

In addition, in the secondary battery 10 according to the presentembodiment, as shown in FIG. 2(a), in the initial stage of using thesecondary battery 10, the potential of the positive electrode 11 tendsto decrease and the potential of the negative electrode 12 tends toincrease immediately before the completion of full discharging.

In addition, the secondary battery 10 according to the presentembodiment, as shown in FIG. 2(a), has a characteristic that thepotential decrease rate of the positive electrode 11 immediately beforethe completion of full discharging is smaller than the potentialincrease rate of the negative electrode 12 immediately before thecompletion of full discharging in the initial stage of using thesecondary battery 10.

That is, the initial stage of using the secondary battery 10 accordingto the present embodiment is, as shown in FIG. 2(a), used under acondition of the potential decrease rate of the positive electrode 11immediately before the completion of full discharging being smaller thanthe potential increase rate of the negative electrode 12 immediatelybefore the completion of full discharging.

In addition, the secondary battery 10 according to the presentembodiment is constituted so that, in the initial stage of using thesecondary battery 10, the absolute value of the potential decrease rateper capacity or per time of the positive electrode 11 immediately beforethe completion of full discharging becomes smaller than the potentialincrease rate of the negative electrode 12 immediately before thecompletion of full discharging.

That is, in the initial stage of using the secondary battery 10, the endof discharging is mainly determined by an increase in the potential ofthe negative electrode 12.

In addition, in the secondary battery 10 according to the presentembodiment, in the initial stage of using the secondary battery, whendischarging is carried out with a constant current of 1/20 C, a ratio(ΔV₂/ΔV₁) of an absolute value (ΔV₂) of an amount of the potentialchanged per 10 mAh/g of the positive electrode 11 immediately before thecompletion of full discharging to an absolute value (ΔV₁) of an amountof the potential changed per 10 mAh/g of the negative electrode 12immediately before the completion of full discharging is preferably setso as to satisfy a relationship ΔV₂/ΔV₁1 and more preferably set so asto satisfy a relationship ΔV₂/ΔV₁≤0.5. That is, the secondary battery 10according to the present embodiment is preferably used under a conditionof, in the initial stage of using the secondary battery, whendischarging is carried out with a constant current of 1/20 C, the ratio(ΔV₂/ΔV₁) of the absolute value (ΔV₂) of the amount of the potentialchanged per 10 mAh/g of the positive electrode 11 immediately before thecompletion of full discharging to the absolute value (ΔV₁) of the amountof the potential changed per 10 mAh/g of the negative electrode 12immediately before the completion of full discharging satisfying therelationship ΔV₂/ΔV₁1 and more preferably used under a condition of theratio satisfying the relationship ΔV₂/ΔV₁≤0.5.

In addition, the secondary battery 10 according to the presentembodiment is designed so that, in the initial stage of using thesecondary battery, when charging is carried out with a constant currentof 1/20 C, a ratio (ΔV₄/ΔV₃) of an absolute value (ΔV₄) of an amount ofthe potential changed per 10 mAh/g of the positive electrode 11immediately before the completion of full charging to an absolute value(ΔV₃) of an amount of the potential changed per 10 mAh/g of the negativeelectrode 12 immediately before the completion of full chargingpreferably satisfies a relationship ΔV₄/ΔV₃1 and more preferablysatisfies a relationship ΔV₄/ΔV₃<0.5. That is, the secondary battery 10according to the present embodiment is preferably used under a conditionof, in the initial stage of using the secondary battery, when chargingis carried out with a constant current of 1/20 C, the ratio (ΔV₄/ΔV₃) ofthe absolute value (ΔV₄) of the amount of the potential changed per 10mAh/g of the positive electrode 11 immediately before the completion offull charging to the absolute value (ΔV₃) of the amount of the potentialchanged per 10 mAh/g of the negative electrode 12 immediately before thecompletion of full charging satisfying the relationship ΔV₄/ΔV₃≤1 andmore preferably used under a condition of the ratio satisfying therelationship ΔV₄/ΔV₃<0.5.

In addition, the secondary battery 10 according to the presentembodiment is preferably continuously used until a state in which, whencharging is carried out with a constant current of 1/20 C, the ratio(ΔV₄/ΔV₃) of the absolute value (ΔV₄) of the amount of the potentialchanged per 10 mAh/g of the positive electrode immediately before thecompletion of full charging to the absolute value (ΔV₃) of the amount ofthe potential changed per 10 mAh/g of the negative electrode immediatelybefore the completion of full charging satisfies a relationshipΔV₄/ΔV₃>1 and more preferably continuously used until a state in whichthe ratio satisfies a relationship ΔV₄/ΔV₃>2.

According to the secondary battery 10 according to the presentembodiment, the charge and discharge characteristics of the positiveelectrode 11 and the negative electrode 12 satisfy the relationshipsshown in FIG. 2(a) in the initial stage of using the secondary battery,and thus, in the initial stage of using the secondary battery 10, it ispossible to make excess conduction ions present in the positiveelectrode 11 at the time of completing full charging. In such a case,the secondary battery 10 according to the present embodiment can beoperated using some of the capacity of the positive electrode 11 and theentire capacity of the negative electrode 12.

Therefore, it is possible to suppress the capacity of the secondarybattery 10 being decreased even when the capacity of the positiveelectrode 11 decreases. In addition, in the period of time of thesecondary battery 10 being used, when some of the conduction ions thatcontribute to charging and discharging decrease due to the absorptioninto the reaction product by the decomposition of the electrolyticsolution or the like, the available portion in the capacity of thepositive electrode 11 shifts, whereby it is possible to compensate forthe decreased conduction ions using the excess conduction ions in thepositive electrode 11. Therefore, it is possible to suppress thecapacity of the secondary battery 10 being decreased even when some ofthe conduction ions that contribute to charging and dischargingdecrease.

In addition, the secondary battery 10 according to the presentembodiment is capable of operating as a battery even when used until astate in which the potential increase rate of the positive electrode 11immediately before the completion of full charging becomes larger thanthe potential decrease rate of the negative electrode 12 immediatelybefore the completion of full charging as shown in FIG. 2(b). Therefore,the secondary battery 10 according to the present embodiment ispreferably continuously used until a state in which the potentialincrease rate of the positive electrode 11 immediately before thecompletion of full charging becomes larger than the potential decreaserate of the negative electrode 12 immediately before the completion offull charging. In such a case, according to the secondary battery 10according to the present embodiment, it is possible to further extendthe product service life.

As a method for realizing a secondary battery in which the charge anddischarge characteristics of the positive electrode 11 and the negativeelectrode 12 satisfy the relationships shown in FIG. 2(a) and FIG. 2(b),for example, a method in which the positive electrode 11 on which atreatment that removes some of the conduction ions in the positiveelectrode 11 has been carried out is used, a method in which thenegative electrode 12 including a material having an irreversiblecapacity is used, a method in which the negative electrode 12 to whichconduction ions have been added is used, a method in which the positiveelectrode 11 to which conduction ions have been added is used, a methodin which the positive electrode 11 on which a chemical treatment thatremoves or adds some of the conduction ions in the positive electrode 11has been carried out is used, and the like are exemplified.

Examples of the material having an irreversible capacity includepolyimides, silicon, and the like. In addition, as the treatment thatadds conduction ions to the positive electrode 11, over dischargingtreatment and the like are exemplified.

As the method for realizing a secondary battery in which the charge anddischarge characteristics of the positive electrode 11 and the negativeelectrode 12 satisfy the relationships shown in FIG. 2(a) and FIG. 2(b),more specifically, the following methods 1 to 4 are exemplified.

(Method 1) A method in which a positive electrode having a largerirreversible capacity than a negative electrode on which a treatmentthat removes some of conduction ions (for example, a chemical treatment)has been carried out is used (refer to Example 1 described below)

(Method 2) A method in which a negative electrode including a negativeelectrode active material having an irreversible capacity that issmaller than the irreversible capacity of a positive electrode and amaterial having an irreversible capacity (for example, a polyimide orsilicon) is used (refer to Example 2 described below)

(Method 3) A method in which a negative electrode having a largerirreversible capacity than a positive electrode on which a treatmentthat adds conduction ions (for example, a chemical treatment) has beencarried out is used (refer to Example 3 described below)

(Method 4) A method in which a positive electrode having a smallerirreversible capacity than a negative electrode on which a treatmentthat adds conduction ions (for example, a chemical treatment or an overdischarging treatment) has been carried out is used (refer to Example 4described below)

It is possible to produce an assembled battery by combining a pluralityof the secondary batteries 10 according to the present embodiment. Thesecondary batteries 10 according to the present embodiment or anassembled battery thereof can be preferably used in the use of storagesystems, automobile batteries, and the like.

In addition, the secondary battery 10 according to the presentembodiment is, for example, a lithium ion secondary battery.

Next, the respective components constituting the secondary battery 10according to the present embodiment will be described.

(Positive Electrode)

The positive electrode 11 that constitutes the secondary battery 10according to the present embodiment has, for example, the positiveelectrode current collector 3 constituted of a metal foil such as analuminum foil and the positive electrode active material layer 1containing a positive electrode active material that is provided on onesurface of the positive electrode current collector 3.

The positive electrode active material is not particularly limited aslong as the positive electrode active material includes a materialcapable of storing and discharging lithium. For example, it is possibleto use 4 V-class (average operating potential=3.6 to 3.8 V; counterlithium potential) materials such as LiMn₂O₄, LiCoO₂, and the like. Inthese positive electrode active materials, the development potential isregulated by a redox reaction of a Co ion or a Mn ion (Co³⁺↔Co⁴⁻ orMn³⁻↔Mn⁴⁺).

In addition, as the positive electrode active material, it is alsopossible to use lithium-containing complex oxides such as LiM1O₂ (M1represents at least one element selected from the group consisting ofMn, Fe, Co, and Ni, and some of M1's may be substituted by Mg, Al, orTi), LiMn_(2-x)M2_(x)O₄ (M2 represents at least one element selectedfrom the group consisting of Mg, Al, Co, Ni, Fe, and B, and 0≤x<0.4),and the like; olivine-type materials represented by LiFePO₄; and thelike.

In addition, from the viewpoint of obtaining a high energy density, apositive electrode active material capable of storing and discharginglithium ions at a potential of equal to or higher than 4.5 V withrespect to lithium metal is preferably included.

The positive electrode active material having a potential that is equalto or higher than 4.5 V with respect to lithium metal can be selectedusing a method as described below. First, a positive electrode includinga positive electrode active material and Li metal are disposed in acontainer in a state of facing each other across a separator, and thenan electrolytic solution is poured into the container, thereby producinga battery. In addition, a positive electrode active material having acharge and discharge capacity of equal to or more than 10 mAh/g per massof the positive electrode active material at a potential that is equalto or higher than 4.5 V with respect to lithium metal in the case ofcarrying out charging and discharging at a constant current thatreaches, for example, 5 mAh/g per mass of the positive electrode activematerial in a positive electrode can be used as the positive electrodeactive material that operates at a potential of equal to or higher than4.5 V with respect to lithium metal.

For example, it is known that a 5 V-class operating potential can berealized using a spinel compound obtained by substituting Mn in lithiummanganite with Ni, Co, Fe, Cu, Cr, or the like as the positive electrodeactive material. Specifically, it is known that a spinel compound suchas LiNi_(0.5)Mn_(1.5)O₄ exhibits a potential flat in a range of equal toor higher than 4.5 V. In the above-described spinel compound, Mn ispresent in a tetravalent state, and the operating potential is regulatedby the redox of Ni²⁺↔Ni⁴⁺ instead of the redox of Mn³⁻↔Mn⁴⁺.

For example, LiNi_(0.5)Mn_(1.5)O₄ has a capacity of equal to or morethan 130 mAh/g and an average operating voltage of equal to or higherthan 4.6 V with respect to lithium metal. The capacity is smaller thanthat of LiCoO₂, but the energy density of a battery is higher than thatof LiCoO₂. Furthermore, spinel-type lithium manganese oxides have athree-dimensional lithium diffusion path and also have advantages ofexcellent thermodynamic stability and easiness of synthesis.

As the positive electrode active material that operates at a potentialof equal to or higher than 4.5 V with respect to lithium metal, forexample, there is a lithium manganese complex oxide represented byFormula (1). The lithium manganese complex oxide represented by Formula(1) is a positive electrode active material that operates at a potentialof equal to or higher than 4.5 V with respect to lithium metal.

Li_(a)(M_(x)Mn_(2-x-y)Y_(y))(O_(4-w)Z_(w))   (1)

(In the formula, 0.3≤x≤1.2, 1≤y, x+y<2, 0≤a≤1.2, and M represents atleast one selected from the group consisting of Co, Ni, Fe, Cr, and Cu.Y represents at least one selected from the group consisting of Li, B,Na, Al, Mg, Ti, Si, K, and Ca. Z is at least one selected from the groupconsisting of F and Cl.)

In addition, the lithium manganese complex oxide represented by Formula(1) is more preferably a compound represented by Formula (1-1).

Li_(a) (M_(x)Mn_(2-x-y)Y_(y))(O_(4-w)Z_(w))   (1-1)

(In the formula, 0.5≤x≤1.2, 0≤y, x+y<2, 0≤a≤1.2, and M represents atleast one selected from the group consisting of Co, Ni, Fe, Cr, and Cu.Y represents at least one selected from the group consisting of Li, B,Na, Al, Mg, Ti, Si, K, and Ca. Z is at least one selected from the groupconsisting of F and Cl.)

In addition, in Formula (1), Ni is preferably included as M, and M ismore preferably only Ni. This is because, in the case of including Ni asM, it is possible to relatively easily obtain positive electrode activematerials having a high capacity. Ina case in which M is only Ni, fromthe viewpoint of obtaining positive electrode active materials having ahigh capacity, x is preferably equal to or more than 0.4 and equal to orless than 0.6. In addition, when the positive electrode active materialis LiNi_(0.5)Mn_(1.5)O₄, a high capacity of equal to or more than 130mAh/g can be obtained, which is more preferable.

In addition, as the positive electrode active material that operates ata potential of equal to or higher than 4.5 V with respect to lithiummetal, which is represented by Formula (1), for example, LiCrMnO₄,LiFeMnO₄, LiCoMnO₄, LiCu_(0.5)Mn_(1.5)O₄, and the like are exemplified.These positive electrode active materials have a high capacity. Inaddition, the positive electrode active material may have a compositionobtained by mixing the above-described active material andLiNi_(0.5)Mn_(1.5)O₄.

In addition, there is a case where it becomes possible to improveservice lives by substituting some of Mn portions in these activematerials with Li, B, Na, Al, Mg, Ti, SiK, Ca, or the like. That is, inFormula (1), there is a case where service lives can be improved in thecase of 0<y. Among these, in a case where Y is Al, Mg, Ti, or Si, theservice life improvement effect is strong. In addition, in a case whereY is Ti, the service life improvement effect is exhibited whilemaintaining a high capacity, which is more preferable. The range of y ispreferably more than 0 and equal to or less than 0.3. When y is set tobe equal to or less than 0.3, it becomes easy to suppress a decrease inthe capacity.

In addition, it is possible to substitute oxygen portions with F or Cl.In Formula (1), when w is set to be more than 0 and equal to or lessthan 1, it is possible to suppress a decrease in the capacity.

As examples of the spinel-type positive electrode active materialrepresented by Formula (1), for example, compounds including Ni as Msuch as LiNi_(0.5)Mn_(1.5)O₄; LiCr_(x)Mn_(2-x)O₄ (0.4≤x≤1.1),LiFe_(x)Mn_(2-x)O₄ (0.4≤x≤1.1), LiCu_(x)Mn_(2-x)O₄ (0.3≤x≤0.6),LiCo_(x)Mn_(2-x)O₄ (0.4≤x≤1.1), and the like; and solid solutionsthereof.

In addition, as the positive electrode active material that operates ata potential of equal to or higher than 4.5 V with respect to lithiummetal, olivine-type positive electrode active materials are exemplified.As the olivine-type positive electrode active materials, LiMPO₄ (M: atleast one of Co and Ni), for example, LiCoPO₄, LiNiPO₄, or the like isexemplified.

In addition, as the positive electrode active material that operates ata potential of equal to or higher than 4.5 V with respect to lithiummetal, Si complex oxides are exemplified, and examples of the Si complexoxides include Li₂MSiO₄ (M: at least one of Mn, Fe, and Co).

In addition, as the positive electrode active material that operates ata potential of equal to or higher than 4.5 V with respect to lithiummetal, positive electrode active materials having a lamellar structureare also exemplified, and examples thereof include positive electrodeactive materials represented by Li (M1_(x)M2_(y)Mn_(2-x-y)) O₂ (M1: atleast one selected from the group consisting of Ni, Co, and Fe, M2: atleast one selected from Li, Mg, and Al, 0.1<x<0.5, and 0.05<y<0.3),Li(M_(1-z)Mn_(z))O₂ (M: at least one selected from the group consistingof Li, Co, and Ni and 0.7≥z≥0.33), Li (Li_(x)M_(2-x-z)Mn_(z)) O₂ (M: atleast one of Co and Ni, 0.3>x≥0.1, and 0.7≥z≥0.33), or the like.

A specific surface area of the positive electrode active material suchas the lithium manganese complex oxide represented by Formula (1) or thelike is, for example, 0.01 to 5 m²/g, preferably 0.05 to 4 m²/g, morepreferably 0.1 to 3 m²/g, and still more preferably 0.2 to 2 m²/g. Whenthe specific surface area is set to the above-described range, it ispossible to adjust a contact area with the electrolytic solution to anappropriate range. That is, when the specific surface area is set to beequal to or more than the above-described lower limit value, it becomeseasy to smoothly insert and desorb lithium ions, and the resistance canbe further decreased. In addition, when the specific surface area is setto be equal to or less than the above-described upper limit value, it ispossible to suppress the decomposition of the electrolytic solutionbeing accelerated or the elution of the constituent elements of theactive material.

A central particle diameter (median diameter: D₅₀) of the activematerial such as the lithium manganese complex oxide or the like ispreferably 0.1 to 50 μm and more preferably 0.2 to 40 μm. When theparticle diameter is set to be equal to or more than the above-describedlower limit value, it is possible to further suppress the elution of theconstituent elements such as Mn and the like and further suppress thedeterioration caused by the contact with the electrolytic solution. Inaddition, when the particle diameter is set to be equal to or less thanthe above-described upper limit value, it becomes easy to smoothlyinsert and desorb lithium ions, and the resistance can be furtherdecreased.

The particle diameter can be measured using a laser diffraction andscattering-type particle size distribution measurement instrument.

The positive electrode active material can be used singly or two or morepositive electrode active materials can be jointly used.

For example, only the above-described 4 V-class positive electrodeactive material may be included. In addition, from the viewpoint ofobtaining a high energy density, it is more preferable to use thepositive electrode active material that operates at a potential of equalto or higher than 4.5 V with respect to lithium metal as describedabove. The 4 V-class positive electrode active material may be furtherincluded.

A binding agent for the positive electrode is not particularly limited,and examples thereof include polyvinylidene fluoride (PVDF), vinylidenefluoride-hexafluoropropylene copolymers, vinylidenefluoride-tetrafluoroethylene copolymers, styrene-butadiene copolymerizedrubber, polytetrafluoroethylene, polypropylene, polyethylene, polyimide,polyamide-imide, and the like. Among these, polyvinylidene fluoride ispreferred from the viewpoint of versatility or a low cost.

The amount of the binding agent for the positive electrode being used ispreferably 2 to 10 parts by mass with respect to 100 parts by mass ofthe positive electrode active material from the viewpoint of “asufficient binding force” and “an increase in energy” that are in atrade-off relationship.

To the positive electrode active material layer 1 including the positiveelectrode active material, a conductive auxiliary agent may be added forthe purpose of decreasing the impedance. Examples of the conductiveauxiliary agent include fine carbonaceous particles such as graphite,carbon black, acetylene black, and the like.

The positive electrode current collector 3 is not particularly limited;however, from the viewpoint of electrochemical stability, a currentcollector constituted of one or more selected from aluminum, nickel,copper, silver, alloys thereof, and stainless steel is preferred. As ashape of the positive electrode current collector 3, for example, afoil, a flat plate shape, a mesh shape, and the like are exemplified.

The positive electrode 11 can be produced by, for example, forming thepositive electrode active material layer 1 including the positiveelectrode active material and the binding agent for the positiveelectrode on the positive electrode current collector 3. As a method forforming the positive electrode active material layer 1, for example, adoctor blade method, a die coater method, a CVD method, a sputteringmethod, and the like are exemplified. The positive electrode currentcollector 3 may also be produced by forming the positive electrodeactive material layer 1 in advance and then forming a thin film ofaluminum, nickel, or an alloy thereof using a method such as deposition,sputtering, or the like.

(Negative Electrode)

The negative electrode 12 that constitutes the secondary battery 10according to the present embodiment has, for example, the negativeelectrode current collector 4 constituted of a metal foil such as acopper foil and the negative electrode active material layer 2containing a negative electrode active material that is provided on onesurface of the negative electrode current collector 4.

The negative electrode active material is not particularly limited aslong as the negative electrode active material includes a materialcapable of storing and discharging lithium, and examples thereof include(a) carbon materials capable of storing and discharging lithium ions,(b) metal capable of storing and discharging lithium, (c) metal oxidescapable of storing and discharging lithium ions, and the like.

As the carbon materials (a), it is possible to use graphite (naturalgraphite, artificial graphite, and the like), amorphous carbon,diamond-like carbon, carbon nanotubes, complexes thereof, and the like.

Here, highly crystalline graphite has a high electric conductionproperty and is excellent in terms of adhesiveness to the negativeelectrode current collector 4 made of metal such as copper and voltageflatness. On the other hand, poorly crystalline amorphous carbon has avolume that expands to a relatively small extent and thus has a strongeffect for alleviating the volume expansion of the entire negativeelectrode and does not easily deteriorate due to non-uniformity such ascrystal grain boundaries or defects.

The carbon material (a) can be used singly or can be jointly used withother substance. In an embodiment in which the carbon material isjointly used with other substance, the content of the carbon material(a) is preferably in a range of equal to or more than 2% by mass andequal to or less than 80% by mass and more preferably in a range ofequal to or more than 2% by mass and equal to or less than 30% by massof the negative electrode active material.

As the metal (b), it is possible to use, for example, metal containing,as a main body, Al, Si, Pb, Sn, Zn, Cd, Sb, In, Bi, Ag, Ba, Ca, Hg, Pd,Pt, Te, La, or the like; alloys of two or more of these metals; alloysof these metals or alloys and lithium; and the like. As the metal (b),silicon (Si) is more preferably included.

The metal (b) can be used singly or can be jointly used with othersubstance. In an embodiment in which the metal is jointly used withother substance, the content of the metal (b) is preferably in a rangeof equal to or more than 5% by mass and equal to or less than 90% bymass and more preferably in a range of equal to or more than 20% by massand equal to or less than 50% by mass of the negative electrode activematerial.

As the metal oxides (c), it is possible to use, for example, siliconoxide, aluminum oxide, tin oxide, indium oxide, zinc oxide, lithiumoxide, complexes thereof, and the like. As the metal oxide (c), siliconoxide is more preferably included. This is because silicon oxide isrelatively stable and does not easily cause a reaction with othercompounds.

In addition, it is also possible to add, for example, 0.1% to 5% by massof one or more elements selected from nitrogen, boron, and sulfur to themetal oxide (c). In such a case, the electric conduction property of themetal oxide (c) can be improved.

The metal oxide (c) can be used singly or can be jointly used with othersubstance. In an embodiment in which the metal oxide is jointly usedwith other substance, the content of the metal oxide (c) is preferablyin a range of equal to or more than 5% by mass and equal to or less than90% by mass and more preferably in a range of equal to or more than 40%by mass and equal to or less than 70% by mass of the negative electrodeactive material.

Examples of the metal oxide (c) include LiFe₂O₃, WO₂, MoO₂, SiO, SiO₂,CuO, SnO, SnO₂, Nb₃O₅, Li_(x)Ti_(2-x)O₄ (1≤x≤4/3), PbO₂, Pb₂O₅, and thelike.

In addition, as the negative electrode active material, in addition tothe above-described materials, for example, (d) metal sulfides capableof storing and discharging lithium ions are exemplified. Examples of themetal sulfides (d) include SnS, FeS₂, and the like.

In addition, as the negative electrode active material, in addition tothe above-described materials, for example, metallic lithium; lithiumalloys; polyacene; polythiophene; lithium nitrides such as Li₅(Li₃N),Li₇MnN₄, Li₃FeN₂, Li_(2.5)Co_(0.5)N, Li₃CoN, and the like; and the likecan be exemplified.

The above-described negative electrode active materials can be usedsingly or two or more negative electrode active materials can be used ina mixture form.

In addition, the negative electrode active material can be constitutedto include the carbon material (a), the metal (b), and the metal oxide(c). Hereinafter, this negative electrode active material will bedescribed.

The metal oxide (c) preferably has an amorphous structure wholly orpartially. The metal oxide (c) having an amorphous structure is capableof suppressing the volume expansion of the carbon material (a) or themetal (b) and is capable of suppressing the decomposition of theelectrolytic solution. Regarding this mechanism, it is assumed that themetal oxide (c) has an amorphous structure, which affects the formationof coatings in the interface between the carbon material (a) and theelectrolytic solution by some means. In addition, in amorphousstructures, it is considered that there are a relatively small number ofelements caused by non-uniformity such as crystal grain boundaries ordefects. Meanwhile, the fact that the metal oxide (c) has an amorphousstructure wholly or partially can be confirmed by an X-ray diffractionmeasurement (ordinary XRD measurement). Specifically, in a case wherethe metal oxide (c) does not have an amorphous structure, an intrinsicpeak of the metal oxide (c) is observed; however, in a case where themetal oxide (c) has an amorphous structure wholly or partially, thebroadened intrinsic peak of the metal oxide (c) is observed.

The metal oxide (c) is preferably an oxide of the metal that constitutesthe metal (b). In addition, the metal (b) and the metal oxide (c) arerespectively preferably silicon (Si) and silicon oxide (SiO).

All or part of the metal (b) is preferably dispersed in the metal oxide(c). When at least part of the metal (b) is dispersed in the metal oxide(c), it is possible to further suppress the volume expansion of theentire negative electrode and also suppress the decomposition of theelectrolytic solution. Meanwhile, the fact that all or part of the metal(b) is dispersed in the metal oxide (c) can be confirmed by jointlyusing a transmission electron microscopic observation (ordinarytransmission electron microscopic (TEM) observation) and an energydispersive X-ray spectrometric (EDX) measurement (ordinary energydispersive X-ray spectroscopic measurement). Specifically, a crosssection of a sample including the particles of the metal (b) isobserved, the oxygen concentration of the particles of the metal (b)dispersed in the metal oxide (c) is measured, and the metal thatconstitutes the particles of the metal (b) not turning into an oxide canbe confirmed.

As described above, the respective content rates of the carbon material(a), the metal (b), and the metal oxide (c) with respect to the total ofthe carbon material (a), the metal (b), and the metal oxide (c) arepreferably equal to or more than 2% by mass and equal to or less than80% by mass, equal to or more than 5% by mass and equal to or less than90% by mass, and equal to or more than 5% by mass and equal to or lessthan 90% by mass, respectively. In addition, the respective contentrates of the carbon material (a), the metal (b), and the metal oxide (c)with respect to the total of the carbon material (a), the metal (b), andthe metal oxide (c) are more preferably equal to or more than 2% by massand equal to or less than 30% by mass, equal to or more than 20% by massand equal to or less than 50% by mass, and equal to or more than 40% bymass and equal to or less than 70% by mass, respectively.

A negative electrode active material in which the metal oxide (c) has anamorphous structure wholly or partially and all or part of the metal (b)is dispersed in the metal oxide (c) can be produced using, for example,a method as disclosed by Japanese Laid-open Patent Publication No.2004-47404. That is, a CVD treatment is carried out on the metal oxide(c) in an atmosphere including an organic substance gas such as methanegas, whereby it is possible to turn the metal (b) in the metal oxide (c)into nanoclusters and obtain a complex having a surface coated with thecarbon material (a). In addition, the negative electrode active materialcan also be produced by mixing the carbon material (a), the metal (b),and the metal oxide (c) by mechanical mixing.

In addition, the carbon material (a), the metal (b), and the metal oxide(c) are not particularly limited, and it is possible to use aparticulate carbon material, a particulate metal, and a particulatemetal oxide respectively. For example, the metal (b) can be constitutedto have an average particle diameter that is smaller than the averageparticle diameter of the carbon material (a) and the average particlediameter of the metal oxide (c). In such a case, the metal (b) having avolume that is significantly changed due to charging and discharging hasa relatively small particle diameter, and the carbon material (a) or themetal oxide (c) having a volume that is slightly changed has arelatively large particle diameter, and thus the generation of dendritesand the pulverization of alloys can be more effectively suppressed.

In addition, in a process of charging and discharging, lithium issequentially stored in and discharged from particles having a largeparticle diameter, particles having a small particle diameter, andparticles having a large particle diameter, which also suppress thegeneration of residual stress or residual strain. The average particlediameter of the metal (b) can be set to, for example, equal to or lessthan 20 μm and is preferably set to equal to or less than 15 μm.

In addition, the average particle diameter of the metal oxide (c) ispreferably equal to or less than ½ of the average particle diameter ofthe carbon material (a), and the average particle diameter of the metal(b) is preferably equal to or less than ½ of the average particlediameter of the metal oxide (c). Furthermore, it is more preferable thatthe average particle diameter of the metal oxide (c) is equal to or lessthan ½ of the average particle diameter of the carbon material (a) andthe average particle diameter of the metal (b) is equal to or less than½ of the average particle diameter of the metal oxide (c). When theaverage particle diameters are controlled to be in the above-describedranges, it is possible to more effectively obtain an effect foralleviating the volume expansion of metal and alloy phases and obtainsecondary batteries being excellent in terms of the balance among theenergy density, the cycle service life, and the efficiency. Morespecifically, it is preferable to set the average particle diameter ofsilicon oxide (c) to be equal to or less than ½ of the average particlediameter of graphite (a) and set the average particle diameter ofsilicon (b) to be equal to or less than ½ of the average particlediameter of silicon oxide (c). In addition, more specifically, theaverage particle diameter of silicon (b) can be set to be equal to orless than 20 μm and is preferably set to equal to or less than 15 μm.

In addition, as the negative electrode active material, it is possibleto use graphite having a surface coated with a poorly crystalline carbonmaterial. When the surface of graphite is coated with a poorlycrystalline carbon material, it is possible to suppress a reactionbetween the negative electrode active material and the electrolyticsolution even in the case of using highly conductive carbon as thenegative electrode active material. Therefore, when the graphite coatedwith a poorly crystalline carbon material is used as the negativeelectrode active material, it is possible to improve the capacityretention of batteries and improve battery capacities.

For the poorly crystalline carbon material that coats the surface ofgraphite, a ratio I_(D)/I_(G) of a peak intensity I_(D) of a D peak thatis generated in a range of 1,300 cm⁻¹ to 1,400 cm⁻¹ to a peak intensityI_(G) of a G peak that is generated in a range of 1,550 cm⁻¹ to 1,650cm⁻¹ in a Raman spectrum obtained by a laser Raman analysis ispreferably equal to or more than 0.08 and equal to or less than 0.5.

Generally, highly crystalline carbon materials exhibit a lowI_(D)/I_(G), and poorly crystalline carbon materials exhibit a highI_(D)/I_(G). When I_(D)/I_(G) is equal to or more than 0.08, even in acase where the negative electrode active material is operated at a highvoltage, it is possible to suppress the reaction between the graphiteand the electrolytic solution and improve the capacity retention ofbatteries. When I_(D)/I_(G) is equal to or less than 0.5, it is possibleto improve battery capacities. In addition, I_(D)/I_(G) is morepreferably equal to or more than 0.1 and equal to or less than 0.4.

For the laser Raman analysis of the poorly crystalline carbon material,it is possible to use, for example, an argon ion laser Raman analyzer.In the case of materials that absorb a large amount of a laser such ascarbon materials, the laser is absorbed into up to several tens ofnanometers from the surface. Therefore, information of the poorlycrystalline carbon material disposed on the surface can be substantiallyobtained by carrying out a laser Raman analysis on the graphite having asurface coated with the poorly crystalline carbon material.

The I_(D) value or the I_(G) value can be obtained from, for example, alaser Raman spectrum measured under the following conditions.

Laser Raman spectrometer: Ramanor T-64000 (manufactured by JobinYvon/Atago Bussan Co., Ltd.)

Measurement mode: Macro Roman

Measurement disposition: 60°

Beam diameter: 100

Light source: Ar+laser/514.5 nm

Laser power: 10 mW

Diffraction grid: Single600 gr/mm

Dispersion: Single21A/mm

Slit: 100 μm

Detector: CCD/Jobin Yvon1024256

The graphite coated with the poorly crystalline carbon material can beobtained by, for example, coating particulate graphite with a poorlycrystalline carbon material. The average particle diameter (volumeaverage: D₅₀) of graphite particles is preferably equal to or more than5 μm and equal to or less than 30 μm. The graphite is preferablycrystalline, and the I_(D)/I_(G) value of the graphite is morepreferably equal to or more than 0.01 and equal to or less than 0.08.

The thickness of the poorly crystalline material is preferably equal toor more than 0.01 μm and equal to or less than 5 μm and more preferablyequal to or more than 0.02 μm and equal to or less than 1 μm.

The average particle diameter (D₅₀) can be measured using, for example,a laser diffraction and scattering particle size distributionmeasurement instrument MICROTRAC MT3300EX (manufactured by Nikkiso Co.,Ltd.).

The poorly crystalline carbon material can be formed on the surface ofthe graphite using, for example, a gas-phase method in which hydrocarbonsuch as propane, acetylene, or the like is thermally decomposed, therebydepositing carbon. In addition, the poorly crystalline carbon materialcan be formed using, for example, a method in which pitch, talc, or thelike is attached to the surface of the graphite and fired at 800° C. to1,500° C.

For the graphite, a layer spacing d₀₀₂ of a 002 plane is preferablyequal to or more than 0.33 nm and equal to or less than 0.34 nm, morepreferably equal to or more than 0.333 nm and equal to or less than0.337 nm, and still more preferably equal to or less than 0.336 nm inthe crystal structure. Highly crystalline graphite as described abovehas a high lithium storage capacity and is capable of improving thecharge and discharge efficiency.

The laser spacing of the graphite can be measured by, for example, X-raydiffraction.

A specific surface area of the graphite coated with the poorlycrystalline carbon material is, for example, 0.01 to 20 m²/g, preferably0.05 to 10 m²/g, more preferably 0.1 to 5 m²/g, and still morepreferably 0.2 to 3 m²/g. When the specific surface area of the graphitecoated with the poorly crystalline carbon material is set to be equal toor more than 0.01 m²/g, it becomes easy to smoothly insert and desorblithium ions, and the resistance can be further decreased. When thespecific surface area of the graphite coated with the poorly crystallinecarbon material is set to be equal to or less than 20 m²/g, it ispossible to further suppress the decomposition of the electrolyticsolution and further suppress the elution of the constituent elements ofthe active material into the electrolyte solution.

The graphite that serves as a base material is preferably highlycrystalline graphite, for example, artificial graphite or naturalgraphite can be used, but the graphite is not particularly limitedthereto. As the poorly crystalline carbon material, for example, coaltar, pitch coke, or a phenolic resin is used, and a poorly crystallinecarbon material mixed with highly crystalline carbon can be used. Amixture is prepared by mixing 5% to 50% by mass of the poorlycrystalline carbon material into highly crystalline carbon. The mixtureis heated at 150° C. to 300° C. and then, furthermore, thermally treatedin a range of 600° C. to 1,500° C. Therefore, thermally-treated graphitehaving a surface coated with the poorly crystalline carbon can beobtained. The thermal treatment is preferably carried out in anatmosphere of an inert gas such as argon, helium, nitrogen, or the like.

The negative electrode active material may include, in addition to thegraphite having a surface coated with the poorly crystalline carbonmaterial, other active materials.

A binding agent for the negative electrode is not particularly limited,and examples thereof include polyvinylidene fluoride (PVdF), vinylidenefluoride-hexafluoropropylene copolymers, vinylidenefluoride-tetrafluoroethylene copolymers, styrene-butadiene copolymerizedrubber, polytetrafluoroethylene, polypropylene, polyethylene, polyimide,polyamide-imide, and the like.

The content rate of the binding agent for the negative electrode ispreferably in a range of 1% to 30% by mass and more preferably 2% to 25%by mass of the total amount of the negative electrode active materialand the binding agent for the negative electrode. When the content rateis set to be equal to or more than the above-described lower limitvalue, the adhesiveness between the negative electrode active materialsor between the negative electrode active material and the currentcollector improves, and the cycle characteristics become favorable. Inaddition, when the content rate is set to be equal to or less than theabove-described upper limit value, the ratio of the negative electrodeactive material improves, and it is possible to improve the capacity ofthe negative electrode.

The negative electrode current collector 4 is not particularly limited;however, from the viewpoint of electrochemical stability, a currentcollector constituted of one or more selected from aluminum, nickel,copper, silver, alloys thereof, and stainless steel is preferred. As ashape of the negative electrode current collector 4, for example, afoil, a flat plate shape, a mesh shape, and the like are exemplified.

The negative electrode 12 can be produced by, for example, forming thenegative electrode active material layer 2 including the negativeelectrode active material and the binding agent for the negativeelectrode on the negative electrode current collector 4. As a method forforming the negative electrode active material layer 2, for example, adoctor blade method, a die coater method, a CVD method, a sputteringmethod, and the like are exemplified. The negative electrode currentcollector 4 may also be produced by forming the negative electrodeactive material layer 2 in advance and then forming a thin film ofaluminum, nickel, or an alloy thereof using a method such as deposition,sputtering, or the like.

(Separation Layer)

As the separation layer 5 that constitutes the secondary battery 10according to the present embodiment, it is possible to use, for example,a separator. Examples of the separator include woven fabrics; non-wovenfabrics; porous polymer films such as polyolefin-based films such aspolyethylene, polypropylene, and the like, polyimide films, porouspolyvinylidene fluoride films, and the like; ion conductivepolymer-electrolyte films; and the like. These separators can be usedsingly or in combination.

In addition, in a case where a solid electrolyte is used as the ionconductor, the solid electrolyte can also be used as the separationlayer 5.

(Ion Conductor)

As the ion conductor that constitutes the secondary battery 10 accordingto the present embodiment, for example, electrolytic solutions includinga supporting electrolyte and a non-aqueous electrolytic solvent, solidelectrolytes, and the like are exemplified.

The non-aqueous electrolytic solvent preferably includes a cyclicpolycarbonate and/or a chain-like carbonate.

The cyclic polycarbonate or the chain-like carbonate has a largerelative permittivity, and thus the addition of the carbonate improvesthe dissociation property of the supporting electrolyte and facilitatesthe imparting of a sufficient conduction property. In addition, thecyclic polycarbonate and the chain-like carbonate are favourable interms of voltage resistance and conductivity and are thus suitable forthe mixing with fluorine-containing esters of phosphoric acid.Furthermore, when a material having an effect for decreasing theviscosity of the electrolytic solution is selected, it is also possibleto improve the ion mobility in the electrolytic solution.

The cyclic carbonate is not particularly limited, and, for example,ethylene carbonate (EC), propylene carbonate (PC), butylene carbonate(BC), vinylene carbonate (VC), and the like can be exemplified.

In addition, the cyclic carbonate includes a fluorinated cycliccarbonate. As the fluorinated cyclic carbonate, it is possible toexemplify, for example, compounds obtained by substituting part or allof hydrogen atoms in ethylene carbonate (EC), propylene carbonate (PC),butylene carbonate (BC), vinylene carbonate (VC), or the like withfluorine atoms and the like.

As the fluorinated cyclic carbonate, more specifically, it is possibleto use 4-fluoro-1,3-dioxolan-2-one, (cis or trans)4,5-difluoro-1,3-dioxolane-2-one, 4,4-difluoro-1,3-dioxolan-2-one,4-fluoro-5-methyl-1,3-dioxolan-2-one, and the like.

Among these, the cyclic carbonate is preferably ethylene carbonate,propylene carbonate, a compound obtained by partially fluorinatingethylene carbonate or propylene carbonate, or the like and morepreferably ethylene carbonate from the viewpoint of voltage resistanceor conductivity. The cyclic carbonate can be used singly or two or morecyclic carbonates can be jointly used.

The content rate of the cyclic carbonate in the non-aqueous electrolyticsolvent is preferably equal to or more than 0.1% by volume, morepreferably equal to or more than 5% by volume, still more preferablyequal to or more than 10% by volume, and particularly preferably equalto or more than 15% by volume from the viewpoint of an effect forincreasing the degree of dissociation of the supporting electrolyte andan effect for increasing the conductivity of the electrolytic solution.In addition, the content rate of the cyclic carbonate in the non-aqueouselectrolytic solvent is preferably equal to or less than 70% by volume,more preferably equal to or less than 50% by volume, and still morepreferably equal to or less than 40% by volume from the viewpoint of aneffect for increasing the degree of dissociation of the supportingelectrolyte and an effect for increasing the conductivity of theelectrolytic solution.

The chain-like carbonate is not particularly limited, and, for example,dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), diethylcarbonate (DEC), dipropyl carbonate (DPC), and the like can beexemplified.

In addition, the chain-like carbonate includes a fluorinated chain-likecarbonate. As the fluorinated chain-like carbonate, it is possible toexemplify, for example, compounds having a structure obtained bysubstituting part or all of hydrogen atoms in ethyl methyl carbonate(EMC), dimethyl carbonate (DMC), diethyl carbonate (DEC), dipropylcarbonate (DPC), or the like with fluorine atoms and the like.

As the fluorinated chain-like carbonate, more specifically, bis(fluoroethyl) carbonate, 3-fluoropropylmethyl carbonate,3,3,3-trifluoropropylmethyl carbonate, 2,2,2-trifluoroethyl methylcarbonate, 2,2,2-trifluoroethyl ethyl carbonate, monofluoromethyl methylcarbonate, methyl 2,2,3,3 tetrafluoropropyl carbonate, ethyl 2,2,3,3tetrafluoropropyl carbonate, bis(2,2,3,3, tetrafluoropropyl) carbonate,bis(2,2,2 trifluoroethyl) carbonate, 1-monofluoroethyl ethyl carbonate,1-monofluoroethyl methyl carbonate, 2-monofluoroethyl methyl carbonate,bis(1-monofluoroethyl) carbonate, bis(2-monofluoroethyl) carbonate,bis(monofluoromethyl) carbonate, and the like are exemplified.

Among these, dimethyl carbonate, 2,2,2-trifluoroethyl methyl carbonate,monofluoromethyl methyl carbonate, methyl 2,2,3,3, tetrafluoropropylcarbonate, and the like are preferred from the viewpoint of voltageresistance and conductivity. The chain-like carbonate can be used singlyor two or more chain-like carbonates can be jointly used.

The chain-like carbonate has an advantage that, in a case where thenumber of carbon atoms in a substituent that is added to a “—OCOO—”structure is small, the viscosity is low. On the other hand, when thenumber of carbon atoms is large, the viscosity of the electrolyticsolution increases, and there is a case where the conduction property ofLi ions degrades. For the above-described reason, the total number ofcarbon atoms in two substituents that are added to the “—OCOO—”structure of the chain-like carbonate is preferably equal to or morethan 2 and equal to or less than 6. In addition, in a case where thesubstituent that is added to the “—OCOO—” structure contains a fluorineatom, the oxidation resistance of the electrolytic solution improves.For the above-described reason, the chain-like carbonate is preferably afluorinated chain-like carbonate represented by Formula (2).

C_(n)H_(2n+1−1)F₁—OCOO—C_(m)H_(2m+1-k)F_(k)   (2)

(In Formula (2), n represents 1, 2 or 3, m represents 1, 2, or 3, 1represents any integer of 0 to 2n+1, k represents any integer of 0 to2m+1, and at least any of 1 and k is an integer of equal to or more than1.)

In the fluorinated chain-like carbonate represented by Formula (2), whenthe amount of fluorine substitution is small, the fluorinated chain-likecarbonate reacts with the positive electrode having a high potential,and thus there is a case where the capacity retention of the batterydecreases or gas is generated. On the other hand, when the amount offluorine substitution is too large, there is a case where thecompatibility of the chain-like carbonate with other solvents degradesor the boiling point of the chain-like carbonate decreases. For theabove-described reason, the amount of fluorine substitution ispreferably equal to or more than 1% and equal to or less than 90%, morepreferably equal to or more than 5% and equal to or less than 85%, andstill more preferably equal to or more than 10% and equal to or lessthan 80%. That is, 1, m, and n in Formula (2) preferably satisfy thefollowing relational expression.

0.01≤(1+k)/(2n+2m+2)≤0.9

The chain-like carbonate has an effect for decreasing the viscosity ofthe electrolytic solution and is capable of increasing the conductivityof the electrolytic solution. From these viewpoints, the content rate ofthe chain-like carbonate in the non-aqueous electrolytic solvent ispreferably equal to or more than 5% by mass, more preferably equal to ormore than 10% by mass, and still more preferably equal to or more than15% by mass . In addition, the content of the chain-like carbonate inthe non-aqueous electrolytic solvent is preferably equal to or less than90% by mass, more preferably equal to or less than 80% by mass, andstill more preferably equal to or less than 70% by mass.

In addition, the content rate of the fluorinated chain-like carbonate isnot particularly limited, but is preferably equal to or more than 0.1%by volume and equal to or less than 70% by volume in the non-aqueouselectrolytic solvent. When the content rate of the fluorinatedchain-like carbonate in the non-aqueous electrolytic solvent is equal toor more than the above-described lower limit value, it is possible todecrease the viscosity of the electrolytic solution and enhances theconduction property. In addition, an effect for enhancing the oxidationresistance is obtained. In addition, when the content rate of thefluorinated chain-like carbonate in the non-aqueous electrolytic solventis equal to or less than the above-described upper limit value, it ispossible to maintain the conduction property of the electrolyticsolution at a high level. In addition, the content rate of thefluorinated chain-like carbonate in the non-aqueous electrolytic solventis more preferably equal to or more than 1% by volume, still morepreferably equal to or more than 5% by volume, and particularlypreferably equal to or more than 10% by volume. In addition, the contentrate of the fluorinated chain-like carbonate in the non-aqueouselectrolytic solvent is more preferably equal to or less than 65% byvolume, still more preferably equal to or less than 60% by volume, andparticularly preferably equal to or less than 55% by volume.

The non-aqueous electrolytic solvent may include a fluorine-containingester of phosphoric acid represented by Formula (3).

(In Formula (3), R₁, R₂, and R₃ each independently represent asubstituted or unsubstituted alkyl group, and at least one of R₁, R₂,and R₃ is a fluorine-containing alkyl group.)

In addition, the non-aqueous electrolytic solvent may include afluorine-containing chain-like ether represented by Formula (4).

A-O-B   (4)

(In Formula (4), A and B each independently represent a substituted orunsubstituted alkyl group, and at least one of A and B is afluorine-containing alkyl group.)

When the above-described non-aqueous electrolytic solvent is used, it ispossible to suppress the volume expansion of the secondary battery 10and improve the capacity retention. A reason therefor is not clear, butis assumed that, in the electrolytic solution containing the non-aqueouselectrolytic solvent, the fluorine-containing ester of phosphoric acidand a fluorine-containing ether serve as oxidation-resistant solvents,and an acid anhydride forms a reaction product on the electrodes,whereby the reaction of the electrolytic solution is suppressed, and thevolume expansion can be suppressed. Furthermore, it is considered thatthe fluorine-containing ester of phosphoric acid and thefluorine-containing ether act in a synergetic manner, whereby it ispossible to make the cycle characteristics more favorable. This is acharacteristic that exhibits a more significant effect during the use orafter the storage of the secondary battery under a long-term charge anddischarge cycle or a high-temperature condition in which thedecomposition of the electrolytic solution becomes a significant problemand during the use of a positive electrode active material having a highpotential.

The content rate of the fluorine-containing ester of phosphoric acidrepresented by Formula (3) that is included in the non-aqueouselectrolytic solvent is not particularly limited, but is preferablyequal to or more than 5% by volume and equal to or less than 95% byvolume in the non-aqueous electrolytic solvent. When the content rate ofthe fluorine-containing ester of phosphoric acid in the non-aqueouselectrolytic solvent is equal to or more than the above-described lowerlimit value, an effect for enhancing the voltage resistance furtherimproves. In addition, when the content rate of the fluorine-containingester of phosphoric acid in the non-aqueous electrolytic solvent isequal to or less than the above-described upper limit value, the ionconduction property of the electrolytic solution improves, and thecharge and discharge rate of the battery becomes more favorable. Inaddition, the content rate of the fluorine-containing ester ofphosphoric acid in the non-aqueous electrolytic solvent is morepreferably equal to or more than 10% by volume. In addition, the contentrate of the fluorine-containing ester of phosphoric acid in thenon-aqueous electrolytic solvent is more preferably equal to or lessthan 70% by volume, still more preferably equal to or less than 60% byvolume, particularly preferably equal to or less than 59% by volume, andparticularly preferably equal to or less than 55% by volume.

In the fluorine-containing ester of phosphoric acid represented byFormula (3), R₁, R₂, and R₃ each independently represent a substitutedor unsubstituted alkyl group, and at least one of R₁, R₂, and R₃ is afluorine-containing alkyl group. The fluorine-containing alkyl grouprefers to an alkyl group having at least one fluorine atom. The numbersof carbon atoms in the alkyl groups as R₁, R₂, and R₃ each areindependently preferably equal to or more than 1 and equal to or lessthan 4 and more preferably equal to or more than 1 and equal to or lessthan 3. This is because, when the number of carbon atoms in the alkylgroup is equal to or less than the above-described upper limit value, anincrease in the viscosity of the electrolytic solution is suppressed, itbecomes easy for the electrolytic solution to penetrate into microporesin the electrodes or the separator, the ion conduction propertyimproves, and the current value in the charge and dischargecharacteristics of the battery becomes favorable.

In addition, in Formula (3), all of R₁, R₂, and R₃ are preferably thefluorine-containing alkyl groups.

In addition, at least one of R₁, R₂, and R₃ is preferably afluorine-containing alkyl group in which equal to or more than 50% ofhydrogen atoms in the corresponding unsubstituted alkyl group aresubstituted with fluorine atoms.

In addition, it is more preferable that all of R₁, R₂, and R₃ arefluorine-containing alkyl groups and R₁, R₂, and R₃ arefluorine-containing alkyl groups in which equal to or more than 50% ofhydrogen atoms in the corresponding unsubstituted alkyl group aresubstituted with fluorine atoms.

This is because, when the content rate of the fluorine atoms is large,the voltage resistance further improves, and it is possible to furtherdecrease the deterioration of the battery capacity after the cycle evenin the case of using a positive electrode active material that operatesat a potential of equal to or higher than 4.5 V with respect to lithiummetal.

In addition, the ratio of fluorine atoms in the substituent includinghydrogen atoms in the fluorine-containing alkyl group is more preferablyequal to or more than 55%.

In addition, R₁ to R₃ may have a substituent other than the fluorineatom, and, as the substituent, at least one selected from the groupconsisting of an amino group, a carboxy group, a hydroxy group, a cyanogroup, and a halogen atom (for example, a chlorine atom or a bromineatom) is exemplified. Meanwhile, the above-described number of carbonatoms conceptually includes the substituent as well.

Examples of the fluorine-containing ester of phosphoric acid includetris(trifluoromethyl) phosphate, tris(trifluoroethyl) phosphate,tris(tetrafluoropropyl) phosphate, tris(pentafluoropropyl) phosphate,tris(heptafluorobutyl) phosphate, tris(octafluoropentyl) phosphate, andthe like.

In addition, examples of the fluorine-containing ester of phosphoricacid include trifluoroethyl dimethyl phosphate, bis(trifluoroethyl)methyl phosphate, bistrifluoroethyl ethyl phosphate, pentafluoropropyldimethyl phosphate, heptafluorobutyl dimethyl phosphate, trifluoroethylmethyl ethyl phosphate, pentafluoropropyl methyl ethyl phosphate,heptafluorobutyl methyl ethyl phosphate, trifluoroethyl methyl propylphosphate, pentafluoropropyl methyl propyl phosphate, heptafluorobutylmethyl propyl phosphate, trifluoroethyl methyl butyl phosphate,pentafluoropropyl methyl butyl phosphate, heptafluorobutyl methyl butylphosphate, trifluoroethyl diethyl phosphate, pentafluoropropyl diethylphosphate, heptafluorobutyl diethyl phosphate, trifluoroethyl ethylpropyl phosphate, pentafluoropropyl ethyl propyl phosphate,heptafluorobutyl ethyl propyl phosphate, trifluoroethyl ethyl butylphosphate, pentafluoropropyl ethyl butyl phosphate, heptafluorobutylethyl butyl phosphate, trifluoroethyl ethyl dipropyl phosphate,pentafluoropropyl dipropyl phosphate, heptafluorobutyl dipropylphosphate, trifluoroethyl propyl butyl phosphate, pentafluoropropylpropyl butyl phosphate, heptafluorobutyl propyl butyl phosphate,trifluoroethyl dibutyl phosphate, pentafluoropropyl dibutyl phosphate,heptafluorobutyl dibutyl phosphate, and the like.

Examples of tris(tetrafluoropropyl) phosphate includetris(2,2,3,3-tetrafluoropropyl) phosphate.

Examples of tris(pentafluoropropyl) phosphate includetris(2,2,3,3,3-pentafluoropropyl) phosphate.

Examples of tris(trifluoroethyl) phosphate includetris(2,2,2-trifluoroethyl) phosphate (hereinafter, also abbreviated asPTTFE) and the like.

Examples of tris(heptafluorobutyl) phosphate includetris(1H,1H-heptafluorobutyl) phosphate and the like.

Examples of tris(octafluoropentyl) phosphate includetris(1H,1H,5H-octafluoropentyl) phosphate and the like.

Among these, tris(2,2,2-trifluoroethyl) phosphate represented by Formula(3-1) is preferred since an effect for suppressing the decomposition ofthe electrolytic solution at a high potential is strong.

The fluorine-containing ester of phosphoric acid can be used singly ortwo or more fluorine-containing esters of phosphoric acid can be jointlyused.

The non-aqueous electrolytic solvent may include an ester of carboxylicacid.

The ester of carboxylic acid is not particularly limited, and examplesthereof include ethyl acetate, methyl propionate, ethyl formate, ethylpropionate, methyl butyrate, ethyl butyrate, methyl acetate, methylformate, and the like.

In addition, the ester of carboxylic acid also includes a fluorinatedester of carboxylic acid, and examples of the fluorinated ester ofcarboxylic acid include compounds having a structure obtained bysubstituting part or all of hydrogen atoms in ethyl acetate, methylpropionate, ethyl formate, ethyl propionate, methyl butyrate, ethylbutyrate, methyl acetate, or methyl formate with fluorine atoms and thelike.

In addition, as the fluorinated ester of carboxylic acid, specifically,ethyl pentafluoropropionate, ethyl 3,3,3-trifluoropropionate, methyl2,2,3,3-tetrafluoropropionate, 2,2-difluoroethyl acetate, methylheptafluoroisobutyrate, methyl 2,3,3,3-tetrafluoropropionate, methylpentafluoropropionate, methyl2-(trifluoromethyl)-3,3,3-trifluoropropionate, ethylheptafluorobutyrate, methyl 3,3,3-trifluoropropionate,2,2,2-trifluoroethyl acetate, isopropyl trifluoroacetate, tert-butyltrifluoroacetate, ethyl 4,4,4-trifluorobutyrate, methyl4,4,4-trifluorobutyrate, butyl 2,2-difluoroacetate, ethyldifluoroacetate, n-butyl trifluoroacetate, 2,2,3,3-tetrafluoropropylacetate, ethyl 3-(trifluoromethyl) butyrate, methyltetrafluoro-2-(methoxy) propionate, 3,3,3 trifluoropropyl3,3,3-trifluoropropionate, methyl difluoroacetate,2,2,3,3-tetrafluoropropyl trifluoroacetate, 1H,1H-heptafluorobutylacetate, methyl heptafluorobutyrate, ethyl trifluoroacetate, and thelike are exemplified.

Among these, the ester of carboxylic acid is preferably ethylpropionate, methyl acetate, methyl 2,2,3,3-tetrafluoropropionate, and2,2,3,3-tetrafluoropropyl trifluoroacetate are preferred. Similar to thechain-like carbonate, the ester of carboxylic acid has an effect fordecreasing the viscosity of the electrolytic solution. Therefore, forexample, the ester of carboxylic acid can be used instead of thechain-like carbonate and also can be jointly used with the chain-likecarbonate.

A chain-like ester of carboxylic acid has a characteristic that, in acase where the number of carbon atoms in a substituent that is added toa “—COO—” structure is small, the viscosity is low, but the boilingpoint also tends to decrease. There is a case where a chain-like esterof carboxylic acid having a low boiling point gasifies during theoperation of the battery at a high temperature. On the other hand, whenthe number of carbon atoms is too large, the viscosity of theelectrolytic solution increases, and there is a case where theconduction property degrades. For the above-described reason, the totalnumber of carbon atoms in two substituents that are added to the “—COO—”structure of the chain-like ester of carboxylic acid is preferably equalto or more than 3 and equal to or less than 8. In addition, in a casewhere the substituent that is added to the “—COO—” structure contains afluorine atom, it is possible to improve the oxidation resistance of theelectrolytic solution. For the above-described reason, the chain-likeester of carboxylic acid is preferably a fluorinated chain-like ester ofcarboxylic acid represented by Formula (5).

C_(n)H_(2n+1−1)F₁ ^(—COO)—C_(m)H_(2m+1−k)F_(k)   (5)

(In Formula (5), n represents 1, 2, 3, or 4, m represents 1, 2, 3, or 4,1 represents any integer of 0 to 2n+1, k represents any integer of 0 to2m+1, and at least any of 1 and k is an integer of equal to or more than1.)

In the fluorinated chain-like ester of carboxylic acid represented byFormula (5), when the amount of fluorine substitution is small, thefluorinated chain-like ester of carboxylic acid reacts with the positiveelectrode having a high potential, and thus there is a case where thecapacity retention of the battery decreases or gas is generated. On theother hand, when the amount of fluorine substitution is too large, thereis a case where the compatibility of the chain-like ester of carboxylicacid with other solvents degrades or the boiling point of the chain-likeester of carboxylic acid decreases. For the above-described reason, theamount of fluorine substitution is preferably equal to or more than 1%and equal to or less than 90%, more preferably equal to or more than 10%and equal to or less than 85%, and still more preferably equal to ormore than 20% and equal to or less than 80%. That is, 1, m, and n inFormula (5) preferably satisfy the following relational expression.

0.01≤(1+k)/(2n+2m+2)≤0.9

The content rate of the ester of carboxylic acid in the non-aqueouselectrolytic solvent is preferably equal to or more than 0.1% by mass,more preferably equal to or more than 0.2% by mass, still morepreferably equal to or more than 0.5% by mass, and particularlypreferably equal to or more than 1% by mass. The content rate of theester of carboxylic acid in the non-aqueous electrolytic solvent ispreferably equal to or less than 50% by mass, more preferably equal toor less than 20% by mass, still more preferably equal to or less than15% by mass, and particularly preferably equal to or less than 10% bymass. When the content rate of the ester of carboxylic acid is set to beequal to or more than the above-described lower limit value, it ispossible to further improve the low-temperature characteristics andfurther improve the conductivity. In addition, when the content rate ofthe ester of carboxylic acid is set to be equal to or less than theabove-described upper limit value, it is possible to mitigate the vaporpressure of the battery becoming too high in the case of being left tostand at a high temperature.

In addition, the content rate of the fluorinated chain-like ester ofcarboxylic acid is not particularly limited, but is preferably equal toor more than 0.1% by volume and equal to or less than 50% by volume inthe non-aqueous electrolytic solvent. When the content rate of thefluorinated chain-like ester of carboxylic acid in the non-aqueouselectrolytic solvent is equal to or more than the above-described lowerlimit value, it is possible to decrease the viscosity of theelectrolytic solution and enhances the conduction property. In addition,an effect for enhancing the oxidation resistance is obtained. Inaddition, when the content rate of the fluorinated chain-like ester ofcarboxylic acid in the non-aqueous electrolytic solvent is equal to orless than the above-described upper limit value, it is possible tomaintain the conduction property of the electrolytic solution at a highlevel and ensure the compatibility of the electrolytic solution. Inaddition, the content rate of the fluorinated chain-like ester ofcarboxylic acid in the non-aqueous electrolytic solvent is morepreferably equal to or more than 1% by volume, still more preferablyequal to or more than 5% by volume, and particularly preferably equal toor more than 10% by volume. In addition, the content rate of thefluorinated chain-like ester of carboxylic acid in the non-aqueouselectrolytic solvent is more preferably equal to or less than 45% byvolume, still more preferably equal to or less than 40% by volume, andparticularly preferably equal to or less than 35% by volume.

The non-aqueous electrolytic solvent may include an alkylenebiscarbonate represented by Formula (6) in addition to thefluorine-containing ester of phosphoric acid. The oxidation resistanceof the alkylene biscarbonate is equal to or slightly stronger than thatof the chain-like carbonate, and thus it is possible to improve thevoltage resistance of the electrolytic solution.

(R₄ and R₆ each independently represent a substituted or unsubstitutedalkyl group. R₅ represents a substituted or unsubstituted alkylenegroup.)

In Formula (6), the alkyl group may be a straight-chain-like orbranched-chain-like alkyl group, and the number of carbon atoms ispreferably 1 to 6 and more preferably 1 to 4. The alkylene group is adivalent saturated hydrocarbon group and may be a straight-chain-like orbranched-chain-like alkylene group, and the number of carbon atoms ispreferably 1 to 4 and more preferably 1 to 3.

Examples of the alkylene biscarbonate represented by Formula (6) include1,2-bis(methoxycarbonyloxy) ethane, 1,2-bis(ethoxycarbonyloxy) ethane,1,2-bis(methoxycarbonyloxy) propane,1-ethoxycarbonyloxy-2-methoxycarbonyloxyethane, and the like. Amongthese, 1,2-bis(methoxycarbonyloxy) ethane is preferred.

The content rate of the alkylene biscarbonate in the non-aqueouselectrolytic solvent is preferably equal to or more than 0.1% by volume,more preferably equal to or more than 0.5% by volume, still morepreferably equal to or more than 1% by volume, and particularlypreferably equal to or more than 1.5% by volume. The content rate of thealkylene biscarbonate in the non-aqueous electrolytic solvent ispreferably equal to or less than 70% by volume, more preferably equal toor less than 60% by volume, still more preferably equal to or less than50% by volume, and particularly preferably equal to or less than 40% byvolume.

The alkylene biscarbonate is a material having a low permittivity.Therefore, the alkylene biscarbonate can be used instead of, forexample, the chain-like carbonate or can be jointly used with thechain-like carbonate.

The non-aqueous electrolytic solvent may include a chain-like ester.

The chain-like ether is not particularly limited, and examples thereofinclude 1,2-ethoxyethane (DEE), ethoxymethoxyethane (EME), and the like.

In addition, as the chain-like ether, a halogenated chain-like estersuch as a fluorine-containing ether may also be included. Thehalogenated chain-like ether has strong oxidation resistance and ispreferably used in the case of the positive electrode that operates at ahigh potential.

The chain-like ether, similar to the chain-like carbonate, has an effectfor decreasing the viscosity of the electrolytic solution.

Therefore, the chain-like ether can be used instead of the chain-likecarbonate and the ester of carboxylic acid and can also be jointly usedwith the chain-like carbonate or the ester of carboxylic acid.

In addition, the content rate of the chain-like ether is notparticularly limited, but is preferably equal to or more than 0.1% byvolume and equal to or less than 70% by volume in the non-aqueouselectrolytic solvent. When the content rate of the chain-like ether inthe non-aqueous electrolytic solvent is equal to or more than 0.1% byvolume, it is possible to decrease the viscosity of the electrolyticsolution and enhances the conduction property. In addition, an effectfor enhancing the oxidation resistance is obtained. In addition, whenthe content rate of the chain-like ether in the non-aqueous electrolyticsolvent is equal to or less than 70% by volume, it is possible tomaintain the conduction property of the electrolytic solution at a highlevel and ensure the compatibility of the electrolytic solution. Inaddition, the content rate of the chain-like ether in the non-aqueouselectrolytic solvent is more preferably equal to or more than 1% byvolume, still more preferably equal to or more than 5% by volume, andparticularly preferably equal to or more than 10% by volume. Inaddition, the content rate of the chain-like ether in the non-aqueouselectrolytic solvent is more preferably equal to or less than 65% byvolume, still more preferably equal to or less than 60% by volume, andparticularly preferably equal to or less than 55% by volume.

The non-aqueous electrolytic solvent may include a sulfone compoundrepresented by Formula (7).

(In the formula, R₁ and R₂ each independently represent a substituted orunsubstituted alkyl group. A carbon atom in R₁ and a carbon atom in R₂may bond together through a single bond or a double bond to form a ringstructure.)

In the sulfone compound represented by Formula (7), the number of carbonatoms n₁ in R₁ and the number of carbon atoms n₂ in R₂ are preferably1≤n₁≤12 and 1≤n₂≤12, more preferably 1≤n₁≤6 and 1n₂≤6, and still morepreferably 1≤n₁≤3 and 1≤n₂≤3 respectively. In addition, the alkyl groupmay be a straight-chain-like, branched-chain-like or cyclic alkyl group.

In R₁ and R₂, examples of a substituent include alkyl groups having 1 to6 carbon atoms (for example, a methyl group, an ethyl group, a propylgroup, an isopropyl group, a butyl group, and an isobutyl group) andaryl groups having 6 to 10 carbon atoms (for example, a phenyl group anda naphthyl group).

In an embodiment, the sulfone compound is more preferably a cyclicsulfone compound represented by Formula (7-1).

(In the formula, R₃ represents a substituted or unsubstituted alkylenegroup.)

In R₃, the number of carbon atoms in the alkylene group is preferably 4to 9 and more preferably 4 to 6.

In R₃, examples of a substituent include alkyl groups having 1 to 6carbon atoms (for example, a methyl group, an ethyl group, a propylgroup, an isopropyl group, and a butyl group), halogen atoms (forexample a chlorine atom, a bromine atom, and a fluorine atom), and thelike.

The cyclic sulfone compound is more preferably a compound represented byFormula (7-2).

(In the formula, m represents an integer of 1 to 6.)

In Formula (7-2), m is an integer of 1 to 6 and preferably an integer of1 to 3.

As the cyclic sulfone compound represented by Formula (7-1), forexample, tetramethylene sulfone (sulfolane), pentamethylene sulfone,hexamethylene sulfone, and the like. In addition, examples of the cyclicsulfone compound having a substituent include 3-methyl sulfolane,2,4-dimethyl sulfolane, and the like.

In addition, the sulfone compound may be a chain-like sulfone compound.Examples of the chain-like sulfone compound include ethyl methylsulfone, ethyl isopropyl sulfone, ethyl isobutyl sulfone, dimethylsulfone, diethyl sulfone, and the like. Among these, ethyl methylsulfone, ethyl isopropyl sulfone, and ethyl isobutyl sulfone arepreferred.

The sulfone compound has compatibility with other solvents such asfluorinated ether compounds and has a relatively high permittivity andis thus excellent in terms of the dissolution/dissociation action oflithium salts. The sulfone compound can be used singly or two or moresulfone compounds can be used in a mixture form.

In the case of including the sulfone compound, the content in thenon-aqueous electrolytic solvent is preferably equal to or more than 1%by volume and equal to or less than 75% by volume and more preferablyequal to or more than 5% by volume and equal to or less than 50% byvolume. When the content of the sulfone compound is equal to or morethan the above-described lower limit value, the compatibility of theelectrolytic solution improves. When the content of the sulfone compoundis too large, the viscosity of the electrolytic solution increases, andthere is a concern that, particularly, the capacity decrease of thecharge and discharge cycle characteristics at room temperature may becaused.

The non-aqueous electrolytic solvent may include an acid anhydride. Thecontent rate of the acid anhydride that is included in the non-aqueouselectrolytic solvent is not particularly limited, but is, generally,preferably equal to or more than 0.01% by mass and less than 10% by massand more preferably equal to or more than 0.1% by mass and less than 5%by mass in the non-aqueous electrolytic solvent. When the content rateof the acid anhydride in the non-aqueous electrolytic solvent is equalto or more than 0.01% by mass, an effect for increasing the capacityretention is obtained, and an effect for suppressing the generation ofgas by the decomposition of the electrolytic solution is obtained. Thecontent rate of the acid anhydride in the non-aqueous electrolyticsolvent is more preferably equal to or more than 0.1% by mass. Inaddition, when the content rate of the acid anhydride in the non-aqueouselectrolytic solvent is less than 10% by mass, it is possible tomaintain a favorable capacity retention, and it is also possible tosuppress the amount of gas generated by the decomposition of the acidanhydride. The content rate of the acid anhydride in the non-aqueouselectrolytic solvent is more preferably equal to or less than 5% bymass. The content rate of the acid anhydride in the non-aqueouselectrolytic solvent is still more preferably equal to or more than 0.5%by mass and particularly preferably equal to or more than 0.8% by mass.In addition, the content rate of the acid anhydride in the non-aqueouselectrolytic solvent is still more preferably equal to or less than 3%by mass and particularly preferably equal to or less than 2% by mass.

As the acid anhydride, for example, a carboxylic anhydride, a sulfonicanhydride, and anhydrides of carboxylic acid and sulfonic acid, and thelike are exemplified.

The acid anhydride in the electrolytic solution is considered to form areaction product on the electrodes to suppress the volume expansion ofthe battery in association with charging and discharging and have aneffect for improving the cycle characteristics. In addition, although itis reasoning, the above-described acid anhydride bonds to moisture inthe electrolytic solution and is thus considered to also have an effectfor suppressing the generation of gas attributed to the moisture.

Examples of the acid anhydride include a chain-like acid anhydriderepresented by Formula (8) and a cyclic acid anhydride represented byFormula (9).

(In Formula (8), two X_(i)' s each independently represent a carbonylgroup (—C(═O)—) or a sulfonyl group (—S(═O)₂—), R¹ and R² eachindependently represent an alkyl group having 1 to 10 carbon atoms, analkenyl group having 2 to 10 carbon atoms, a cycloalkyl group having 3to 10 carbon atoms, an aryl group having 6 to 18 carbon atoms, or anaryl alkyl group having 7 to 20 carbon atoms, and at least one hydrogenatom in R₁ and R₂ may be substituted with a halogen atom.)

(In Formula (9), two X₂'s each independently represent a carbonyl group(—C(═O)—) or a sulfonyl group (—S(═O)₂—), R³ represents an alkylenegroup having 1 to 10 carbon atoms, an alkenylene group having 2 to 10carbon atoms, an arylene group having 6 to 12 carbon atoms, acycloalkylene group having 3 to 12 carbon atoms, a cycloalkenylene grouphaving 3 to 12 carbon atoms, or a heterocycloalkylene group having 3 to10 carbon atoms, and at least one hydrogen atom in R³ may be substitutedwith a halogen atom.)

The groups represented by R¹, R², and R³ in Formula (8) and Formula (9)will be described below.

In Formula (8), the alkyl group and the alkenyl group each may be astraight chain or may have a branched chain, and the number of carbonatoms is generally 1 to 10, preferably 1 to 8, and more preferably 1 to5.

In Formula (8), the number of carbon atoms in the cycloalkyl group ispreferably 3 to 10 and more preferably 3 to 6.

In Formula (8), the number of carbon atoms in the aryl group ispreferably 6 to 18 and more preferably 6 to 12. Examples of the arylgroup include a phenyl group, a naphthyl group, and the like.

In Formula (8), the number of carbon atoms in the aryl alkyl group ispreferably 7 to 20 and more preferably 7 to 14. Examples of the arylalkyl group include a benzyl group, a phenylethyl group, a naphthylmethyl group, and the like.

In Formula (8), R¹ and R² each are independently an alkyl group having 1to 3 carbon atoms or a phenyl group.

In Formula (9), the alkylene group and the alkenylene group each may bea straight chain or may have a branched chain, and the number of carbonatoms is generally 1 to 10, preferably 1 to 8, and more preferably 1 to5.

In Formula (9), the number of carbon atoms in the alkylene group ispreferably 6 to 20 and more preferably 6 to 12. Examples of the arylenegroup include a phenylene group, a naphthylene group, a biphenylenegroup, and the like.

In Formula (9), the number of carbon atoms in the cycloalkylene group isgenerally 3 to 12, preferably 3 to 10, and more preferably 3 to 8. Thecycloalkylene group may be a monocycle or may have a plurality of ringstructures like a bicycloalkylene group.

In Formula (9), the number of carbon atoms in the cycloalkenylene groupis generally, 3 to 12, preferably 3 to 10, and more preferably 3 to 8.The cycloalkenylene group may be a monocycle or may have a plurality ofring structures in which at least one ring has an unsaturated bond likea bicycloalkenylene group. Examples of the cycloalkenylene group includedivalent groups formed of cyclohexene, bicycle[2.2.1]heptane,bicycle[2.2.2]octane, or the like.

In Formula (9), the heterocycloalkylene group represents a divalentgroup in which at least one carbon atom on the ring of a cycloalkylenegroup is substituted with one or more hetero atoms such as sulfur,oxygen, nitrogen, and the like. The heterocycloalkylene group ispreferably a 3- to 10-membered ring, more preferably a 4- to 8-memberedring, and still more preferably a 5- or 6-membered ring.

In Formula (9), R³ is more preferably an alkylene group having 1 to 3carbon atoms, an alkenylene group having 2 or 3 carbon atoms, acyclohexylene group, a cyclhexynylene group, or a phenylene group.

The acid anhydride may be partially halogenated. Examples of a halogenatom include chlorine, iodine, bromine, fluorine, and the like, and,among these, chlorine and fluorine are preferred, and fluorine is morepreferred.

In addition, the acid anhydride represented by Formula (8) or Formula(9) may have a non-halogen substituent. As the substituent, alkyl grouphaving 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms,an alkoxy group having 1 to 5 carbon atoms, an aryl group having 6 to 12carbon atoms, an amino group, a carboxy group, a hydroxy group, a cyanogroup, and the like, but the substituent is not limited thereto. Forexample, at least one hydrogen atom in a saturated or unsaturatedhydrocarbon ring that is included in R¹, R², or R³ may be substitutedwith an alkyl group having 1 to 3 carbon atoms.

Examples of the carboxylic anhydride include chain-like acid anhydridessuch as acetic anhydride, propionic anhydride, butyric anhydride,crotonic anhydride, benzoic anhydride, and the like; acid anhydrideshaving a ring structure (cyclic acid anhydrides) such as succinicanhydride, glutaric anhydride, maleic anhydride, phthalic anhydride,5,6-dihydroxy-1,4-dithiin-2,3 dicarboxylic anhydride,5-norbornene-2,3-dicarboxylic anhydride, 1,2,3,6-tetrahydrophthalicanhydride, and bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic anhydride, andthe like; and the like.

In addition, as halides, for example, difluoroacetic anhydride,3H-perfluoropropanoic anhydride, 3,3,3-trifluoropropionic anhydride,pentafluoropropionic anhydride, 2,2,3,3,4,4-hexafluoropentanedioicanhydride, tetrafluorosuccinic anhydride, trifluoroacetic anhydride, andthe like are exemplified. In addition, it is also possible to use acidanhydrides having other substituent such as 4-methylphthalic anhydridein addition to the halides.

Examples of the sulfonic anhydride include chain-like sulfonicanhydrides such as methanesulfonic anhydride, ethanesulfonic anhydride,propanesulfonic anhydride, butanesulfonic anhydride, pentanesulfonicanhydride, hexanesulfonic anhydride, vinylsulfonic anhydride,benzenesulfonic acid anhydride, and the like; cyclic sulfonic anhydridessuch as 1,2-ethanedisulfonic anhydride, 1,3-propane disulfonicanhydride, 1,4-butanedisulfonic anhydride, 1,2-benzenedisulfonicanhydride, and the like; halides thereof; and the like.

Examples of the anhydrides of carboxylic acid and sulfonic acid includechain-like acid anhydrides such as acetic acid methanesulfonicanhydride, acetic acid ethanesulfonic anhydride, acetic acidpropanesulfonic anhydride, propionic acid methanesulfonic anhydride,propionic acid ethanesulfonic anhydride, propionic acid propanesulfonicanhydride, and the like; cyclic acid anhydrides such as 3-sulfopropionicanhydride, 2-methyl-3-sulfopropionic anhydride,2,2-dimethyl-3-sulfopropionic anhydride, 2-ethyl-3-sulfopropionicanhydride, 2,2-diethyl-3-sulfopropionic anhydride, 2-sulfobenzoicanhydride, and the like; halides thereof; and the like.

Among these, the acid anhydride is preferably a carboxylic anhydridehaving a structure represented by [—(C═O)—O—(C═O)—] in the molecule.Examples of the carboxylic anhydride include a chain-like carboxylicanhydride represented by Formula (8-1) and a cyclic carboxylic anhydriderepresented by Formula (9-1).

Meanwhile, groups represented by R¹, R², and R³ in Formula (8-1) andFormula (9-1) are identical to those exemplified in Formula (8) andFormula (9).

As examples of a preferred compound of the acid anhydride, aceticanhydride, maleic anhydride, phthalic anhydride, propionic anhydride,succinic anhydride, benzoic anhydride,5,6-dihydroxy-1,4-dithiin-2,3-dicarboxylic acid,5-norbornene-tetrahydrophthalic anhydride,bicyclo[2.2.2]oct-5-ene-2,3-dicarboxylic anhydride, and the like; acidanhydrides having a halogen or other substituent such as difluoroaceticanhydride, 3H-perfluoropropionic anhydride, trifluoropropionicanhydride, pentafluoropropionic anhydride,2,2,3,3,4,4-hexafluoropentanedioic anhydride, tetrafluorosuccinicanhydride, trifluoroacetic anhydride, 4-methylphthalic anhydride, andthe like; and the like.

The non-aqueous electrolytic solvent may also include the followingsubstance in addition to the above-described substance. The non-aqueouselectrolytic solvent may include, for example, γ-lactones such asγ-butyrolactone, cyclic ethers such as tetrahydrofuran,2-methyltetrahydrofuran, and the like, and the like. In addition, thenon-aqueous electrolytic solvent may include a substance obtained bysubstituting some of hydrogen atoms in the above-described material withfluorine atoms. In addition, additionally, the non-aqueous electrolyticsolvent may also include an aprotic organic solvent such as dimethylsulfoxide, 1,3-dioxolane, formamide, acetamide, dimethylformamide,dioxolane, acetonitrile, propylnitrile, nitromethane, ethyl monoglyme,trimethoxymethane, a dioxolane derivative, methylsulfolane,1,3-dimethyl-2-imidazolidinone, 3-methyl-2-oxazolidinone, a propylenecarbonate derivative, a tetrahydrofuran derivative, ethyl ether,1,3-propane sultone, anisole, or N-methylpyrrolidone. In addition, thenon-aqueous electrolytic solvent may include a cyclic ester of sulfonicacid. For example, a cyclic ester of monosulfonic acid is preferably acompound represented by Formula (10).

(In Formula (10), R₁₀₁ and R₁₀₂ each independently represent a hydrogenatom, a fluorine atom, or an alkyl group having 1 to 4 carbon atoms. nrepresents 0, 1, 2, 3, or 4.)

In addition, for example, a cyclic ester of disulfonic acid ispreferably a compound represented by Formula (10-1).

(In Formula (10-1), R₂₀₁ and R₂₀₄ each independently represent ahydrogen atom, a fluorine atom, or an alkyl group having 1 to 4 carbonatoms. n represents 0, 1, 2, 3, or 4.)

Examples of the cyclic ester of sulfonic acid include esters ofmonosulfonic acid such as 1,3-propane sultone, 1,2-propane sultone,1,4-butane sultone, 1,2-butane sultone, 1,3-butane sultone, 2,4-butanesultone, 1,3-pentane sultone, and the like, esters of disulfonic acidsuch as esters of methylene methane disulfonic acid, esters of ethylenemethane disulfonic acid, and the like, and the like. Among these, as1,3-propane sultone, 1,4-butane sultone, and esters of methylene methanedisulfonic acid are preferred.

The content of the cyclic ester of sulfonic acid in the electrolyticsolution is preferably 0.01% to 10% by mass and more preferably 0.1% to5% by mass. In a case where the content of the cyclic ester of sulfonicacid is equal to or more than 0.01% by mass, it is possible to moreeffectively form a coat on the surface of the positive electrode andsuppress the decomposition of the electrolytic solution.

As the supporting electrolyte, for example, lithium salts such as LiPF₆,LiAsF₆, LiAlCl₄, LiClO₄, LiBF₄, LiSbF₆, LiCF₃SO₃, LiC₄F₉CO₃, LiC(CF₃SO₂)₂, LiN (CF₃SO₂)₂, LiN(C₂F₅SO₂)₂, LiB₁₀Cl₁₀, and the like areexemplified. In addition, as the supporting electrolyte, additionally,lower aliphatic carboxylic acid lithium carboxylate, chloroboranelithium, tetraphenyl borate lithium, LiBr, LiI, LiSCN, LiCl, and thelike. The supporting electrolyte can be used singly or two or moresupporting electrolytes can be used in combination.

In addition, it is possible to add an ion conductive polymer to thenon-aqueous electrolytic solvent. As the ion conductive polymer, forexample, polyethers such as polyethylene oxide, polypropylene oxide, andthe like, polyolefins such as polyethylene, polypropylene, and the like,and the like. In addition, as the ion conductive polymer, for example,polyvinylidene fluoride, polytetrafluoroethylene, polyvinyl fluoride,polyvinyl chloride, polyvinylidene chloride, polymethyl methacrylate,polymethyl acrylate, polyvinyl alcohol, polymethacrylonitrile, polyvinylacetate, polyvinyl pyrrolidone, polycarbonate, polyethyleneterephthalate, polyhexamethylene adipamide, polycaprolactam,polyurethane, polyethyleneimine, polybutadiene, polystyrene, orpolyisoprene, or derivatives thereof. The ion conductive polymer can beused singly or two or more ion conductive polymers can be used incombination. In addition, a polymer including a variety of monomers thatconstitute the above-described polymer may be used.

The solid electrolyte is not particularly specified as long as the solidelectrolyte has a function of a solid electrolyte, and it is possible touse, for example, Na-β-Al₂₀₃, polyethylene oxide (PEO) that is apolymeric solid electrolyte, an oxide ion conductor called a lithiumsuperionic conductor (LISICON), or a sulfide-based solid electrolyte(thio-LISICON or the like).

(Shape of Secondary Battery)

As a shape of the secondary battery 10 according to the presentembodiment, for example, a cylindrical shape, a square shape, a coinshape, a button shape, a laminate shape, and the like are exemplified.As the exterior bodies 6 and 7 of the secondary battery 10, for example,stainless steel, iron, aluminum, titanium, alloys thereof, platedproducts thereof, and the like. As plating, it is possible to use, forexample, nickel plating.

In addition, as a laminate resin film that is used for the laminateshape, for example, aluminum, an aluminum alloy, a titanium foil, andthe like are exemplified. As a material of a thermally fused portion ofa metal laminate resin film, for example, thermoplastic polymericmaterials such as polyethylene, polypropylene, and polyethyleneterephthalate are exemplified. In addition, the numbers of metallaminate resin layers or metal foil layers each are not limited to oneand may be two or more.

As the exterior bodies 6 and 7, any exterior bodies can be appropriatelyselected as long as the exterior bodies are stable to the electrolyticsolution and have a sufficient water vapor barrier property. Forexample, in the case of a laminate-type secondary battery, it ispossible to use, for example, laminate films of polypropylene,polyethylene, or the like coated with aluminum or silica as the exteriorbodies. Particularly, from the viewpoint of suppressing the volumeexpansion, an aluminum laminate film is preferably used.

EXAMPLES

Hereinafter, specific examples to which the present invention is appliedwill be described, but the present invention is not limited to thepresent examples and can be appropriately modified and carried outwithin the scope of the gist of the present invention.

Example 1

As a negative electrode active material of the present example,artificial graphite coated with a poorly crystalline carbon material isused. The artificial graphite coated with a poorly crystalline carbonmaterial, a conductive auxiliary agent that is a spherical carbonmaterial, and a binding agent for a negative electrode are mixedtogether in a mass ratio of 97.7/0.3/2 and dispersed inN-methylpyrrolidone, thereby preparing a slurry for a negativeelectrode. The slurry for a negative electrode is uniformly applied ontoa 10 μm-thick Cu current collector. The slurry for a negative electrodeis dried and then compressed using a roll press, thereby producing anegative electrode.

As a non-aqueous electrolytic solvent, a solvent obtained by mixingethylene carbonate (EC) and diethylene carbonate (DEC) in a volume ratioof 3/7 is used. Hereinafter, the present solvent will be alsoabbreviated as the solvent EC/DEC. LiPF₆ is dissolved in thisnon-aqueous electrolytic solvent in a concentration of 1 mol/L, therebypreparing an electrolytic solution.

A solid solution of LiNiO₂ and Li₂MnO₃ that are positive electrodeactive materials, polyvinylidene fluoride (4% by mass) that is a bindingagent for a positive electrode, and carbon black that is a conductiveauxiliary agent are mixed together, thereby preparing a positiveelectrode mixture. The positive electrode mixture is dispersed inN-methyl-2-pyrrolidone (NMP), thereby preparing a slurry for a positiveelectrode in which PVDF is uniformly dispersed in a NMP solution. Theslurry for a positive electrode is uniformly applied to both surfaces ofa 20 μm-thick aluminum positive electrode current collector. Coatinglayers of the slurry for a positive electrode are dried and thencompressed using a roll press, thereby forming a positive electrodeactive material and producing a positive electrode.

A relationship between first-time charge and discharge curves of theobtained negative electrode and the obtained positive electrode whenboth electrodes are combined together is shown in FIG. 3. In the presentconstitution, the positive electrode has a larger irreversible capacitythan the negative electrode, and thus there is “misalignment” comparedto the target positional relationship of FIG. 2, and a treatment thatcorrects the misalignment becomes necessary.

As one method, there is a method in which lithium in the positiveelectrode is consumed. For example, the positive electrode is immersedand reacted in a NO₂BF₄ solution, thereby chemically desorbing lithiumfrom the positive electrode and removing a capacity of lithium from thepositive electrode as much as the misalignment. A condition for removinga desired amount of lithium is determined by evaluating a relationshipamong the amount removed, the concentration of the solution, and theimmersion time in advance. When the negative electrode and the positiveelectrode on which the above-described treatment has been carried outare combined together, the discharge curves of the positive and negativeelectrodes have a relationship of FIG. 4, and it is possible to matchthe relationship to the relationship of FIG. 2 from the first-timedischarge.

As a separator for separating the positive electrode and the negativeelectrode, a 25 μm-thick microporous polypropylene film is used.

The positive electrode, the negative electrode, and the separator thathave been produced as described above are respectively worked topredetermined shapes, thereby preparing a positive electrode havingpositive electrode active material layers on both surfaces, a negativeelectrode having negative electrode active material layers on bothsurfaces, and the separator. A plurality of the positive electrodes anda plurality of the negative electrodes are respectively laminatedthrough the separators, thereby assembling an electrode element. Theobtained electrode element is encased with an aluminum laminate filmthat is an exterior body, and the electrolytic solution is injectedthereinto. After that, the aluminum laminate film is sealed in, forexample, a reduced-pressure atmosphere of 0.1 atmospheres, whereby it ispossible to produce a lithium ion secondary battery. A positiveelectrode tab is connected to the positive electrode current collectorin the positive electrode, and a negative electrode tab is connected tothe negative electrode current collector in the negative electrode,thereby forming a state in which the positive electrode and the negativeelectrode can be respectively electrically connected from the outside ofthe exterior body through the positive electrode tab and the negativeelectrode tab.

The positive and negative electrode charge and discharge characteristicsof the present lithium ion secondary battery has the relationship ofFIG. 2 in the initial stage of using the product, and thus charging endsby a decrease in the potential of the negative electrode, anddischarging ends by an increase in the potential of the negativeelectrode. In a case where lithium ions are lost due to a decompositionreaction of the electrolytic solution during the charge and dischargecycle or a reaction with an eluted electrode component, lithium in thepositive electrode is discharged until the charging of the negativeelectrode is completed, and thus the capacity seldom changes. At thistime, in the relationship between the positive and negative electrodecharacteristics, the charge and discharge curve of the positiveelectrode is shifted to the left with respect to the charge anddischarge curve of the negative electrode. As the shift proceeds, theamount of the potential of the positive electrode increased duringcharging gradually increases, and, in the end, the end of charging isdetermined by an increase in the potential of the positive electrode. Insuch a case, the capacity begins to decrease in association with theshift, but the battery can be used until the capacity reaches a capacitylower limit necessary for the use of the battery. As such, the presentexample enables the realization of a battery having a long service life.

Example 2

As a negative electrode material of the present example, the material inExample 1 and a polyimide are mixed together. A slurry for a negativeelectrode is uniformly applied onto a 10 μm-thick Cu current collector.The slurry for a negative electrode is dried, then, thermally treated at200° C. for two hours, and then compressed using a roll press, therebyproducing a negative electrode.

A non-aqueous electrolytic solvent and a positive electrode are producedin the same manner as in Example 1. However, the chemical lithiumdesorption treatment is not carried out on the positive electrode.

As a separator for separating the positive electrode and the negativeelectrode, a 20 μm-thick laminate film of microporous polyethylene andaramid is used.

A method for producing a lithium ion secondary battery is identical tothat in Example 1.

In the present example, the polyimide in the negative electrode has acharacteristic of irreversibly storing some of lithium, and thus, out oflithium inserted into the negative electrode from the positiveelectrode, lithium that is stored in the polyimide is deactivated. Whenthe relationship between the amount of the polyimide and the amount oflithium deactivated is evaluated, it is possible to remove a desiredamount of lithium, the misalignment in FIG. 3 is adjusted, and therelationship of the positive and negative electrode charge and dischargecharacteristic of FIG. 5 can be realized.

In the present example, the amount of lithium removed can be controlledusing the amounts of the materials mixed, and thus there is an advantagethat the manufacturing is easy.

Comparative Example 1

Comparative Example 1 is a lithium ion secondary battery in which theconstitution is identical to that in Example 1, but the chemical lithiumdesorption treatment is not carried out on the positive electrode.

At this time, the relationship of the charge and discharge curve betweenthe positive electrode and the negative electrode becomes as shown inFIG. 3. In this case, the amount of lithium ions that are dischargedfrom the positive electrode is larger than the capacity of the negativeelectrode, and thus lithium ions are precipitated on the negativeelectrode, and thus there is a possibility that the negative electrodemay be short-circuited with the positive electrode and the generation ofsmoke or ignition may be caused.

Example 3

As a negative electrode active material of the present example, SiOcoated with a poorly crystalline carbon material is used. SiO, aconductive auxiliary agent that is a spherical carbon material, aconductive auxiliary agent that is a flake-like carbon material, and apolyimide are mixed together and dispersed in N-methylpyrrolidone,thereby preparing a slurry for a negative electrode. The slurry for anegative electrode is uniformly applied onto a 10 μm-thick stainlesssteel current collector. The slurry for a negative electrode is dried,then, thermally treated at 240° C. for one hour, and compressed using aroll press, thereby producing a negative electrode.

As a non-aqueous electrolytic solvent, the same non-aqueous electrolyticsolvent as in Example 1 is used.

LiNi_(0.85)Co_(0.10)Al_(0.05)O₂ that is a positive electrode activematerial, polyvinylidene fluoride (4% by mass) that is a binding agentfor a positive electrode, and carbon black that is a conductiveauxiliary agent are mixed together, thereby preparing a positiveelectrode mixture. The positive electrode mixture is dispersed inN-methyl-2-pyrrolidone, thereby preparing a slurry for a positiveelectrode in which the positive electrode active material and the carbonblack are uniformly dispersed in an NMP solution of PVDF. The slurry fora positive electrode is uniformly applied to both surfaces of a 20μm-thick aluminum positive electrode current collector. Coating layersof the slurry for a positive electrode are dried and then compressedusing a roll press, thereby forming a positive electrode active materialand producing a positive electrode.

A relationship between first-time charge and discharge curves of theobtained negative electrode and the obtained positive electrode whenboth electrodes are combined together is shown in FIG. 6. In the presentconstitution, the negative electrode has a larger irreversible capacitythan the positive electrode, and thus there is “misalignment” comparedto the target positional relationship of FIG. 2, and a treatment thatcorrects the misalignment becomes necessary.

As one method, there is a method in which lithium is added to thenegative electrode before assembly. For example, there is a method inwhich Li is deposited on a surface of the negative electrode anddispersed by a thermal treatment, a method in which a negative electrodeis immersed in an electrolytic solution in which Li metal is disposed asa positive electrode, and a potential is imparted between the positiveand negative electrodes, thereby storing Li in the negative electrode,or the like. The amount of lithium added is controlled by evaluating arelationship among the amount of lithium, the amount of a current, andthe immersion time in advance. When the negative electrode and thepositive electrode on which the above-described treatment has beencarried out are combined together, the discharge curves of the positiveand negative electrodes have a relationship of FIG. 7, and it ispossible to match the relationship to the relationship of FIG. 2 fromthe first-time discharge.

As a separator for separating the positive and negative electrodes, a 25μm-thick microporous polyethylene film is used.

A lithium ion secondary battery is produced in the same manner as inExample 1.

In the present example, in a case where the irreversible capacity of thenegative electrode is large and, in such a state, the relationshipbetween the positive and negative electrodes becomes as shown in FIG. 6,it becomes possible to correct the relationship to the relationship ofFIG. 2.

Example 4

A negative electrode in the present example is identical to that inExample 3.

LiNi_(0.5)Mn_(1.5)O₄ exhibits that is a positive electrode activematerial, polyvinylidene fluoride (4% by mass) that is a binding agentfor a positive electrode, and carbon black that is a conductiveauxiliary agent are mixed together, thereby preparing a positiveelectrode mixture.

Ina case where the obtained negative electrode and the obtained positiveelectrode are used as they are, the charge and discharge curves of thepositive and negative electrodes becomes the relationship of FIG. 6. Asa method for correcting misalignment, there is a method in which lithiumis added to the positive electrode before assembly. For example, apositive electrode is placed in an electrolytic solution in which Limetal is disposed as a negative electrode, a voltage is applied betweenthe positive and negative electrodes, and the positive and negativeelectrodes are further discharged. A positive electrode material in thepresent example has a capacity in a discharge range, and thus lithium isstored.

A non-aqueous electrolytic solvent is produced in the same manner as inExample 1.

As a separator for separating the positive and negative electrodes, a 20μm-thick laminate film of microporous polyethylene and aramid is used.

A method for producing a lithium ion secondary battery is identical tothat in Example 1.

In the present example, the battery is formed after the positiveelectrode is over-discharged, whereby the misalignment of FIG. 6 isadjusted, and the relationship is corrected to a relationship of FIG. 8,whereby it is possible to match the relationship to the relationship ofFIG. 2 from the first-time discharge.

Comparative Example 2

Comparative Example 2 is a lithium ion secondary battery in which theconstitution is identical to that in Example 3, but lithium is not addedto the negative electrode.

At this time, the relationship of the charge and discharge curve betweenthe positive electrode and the negative electrode becomes as shown inFIG. 6. In this case, when lithium is absorbed and lost in a substancegenerated by the decomposition of the electrolytic solution during thecharge and discharge cycle, lithium that is inserted into the positiveelectrode during discharging decreases, and thus the capacity decreases.

Hitherto, the present invention has been described with reference to theembodiments and the examples, but the present invention is not limitedto the embodiment and the examples. The constitution or detail of thepresent invention can be modified in diverse manners that a personskilled in the art can understand within the scope of the presentinvention.

Priority is claimed on the basis of Japanese Patent Application No.2017-031350, filed on Feb. 22, 2017, the content of which isincorporated herein by reference.

1. A secondary battery comprising at least: a positive electrode; anegative electrode; a separation layer that spatially separates thepositive electrode and the negative electrode; and an ion conductor thatis held between the positive electrode and the negative electrode andhas a function of conducting ions between the positive electrode and thenegative electrode, wherein, in an initial stage of using the secondarybattery, the secondary battery has a characteristic of a potentialincrease rate of the positive electrode immediately before completion offull charging being smaller than a potential decrease rate of thenegative electrode immediately before the completion of full chargingand a characteristic of a potential decrease rate of the positiveelectrode immediately before completion of full discharging beingsmaller than a potential increase rate of the negative electrodeimmediately before the completion of full discharging.
 2. The secondarybattery according to claim 1, wherein the secondary battery iscontinuously used until a state in which the potential increase rate ofthe positive electrode immediately before the completion of fullcharging becomes larger than the potential decrease rate of the negativeelectrode immediately before the completion of full charging.
 3. Thesecondary battery according to claim 1, wherein, in the initial stage ofusing the secondary battery, when discharging is carried out with aconstant current of 1/20 C, a ratio (ΔV₂/ΔV₁) of an absolute value (ΔV₂)of an amount of a potential changed per 10 mAh/g of the positiveelectrode immediately before the completion of full discharging to anabsolute value (ΔV₁) of an amount of a potential changed per 10 mAh/g ofthe negative electrode immediately before the completion of fulldischarging satisfies a relationship ΔV₂/ΔV₁<1.
 4. The secondary batteryaccording to claim 1, wherein, in the initial stage of using thesecondary battery, when charging is carried out with a constant currentof 1/20 C, a ratio (ΔV₄/ΔV₃) of an absolute value (ΔV₄) of an amount ofa potential changed per 10 mAh/g of the positive electrode immediatelybefore the completion of full charging to an absolute value (ΔV₃) of anamount of a potential changed per 10 mAh/g of the negative electrodeimmediately before the completion of full charging satisfies arelationship ΔV₄/ΔV₃<1.
 5. The secondary battery according to claim 1,wherein the secondary battery is continuously used until a state inwhich, when charging is carried out with a constant current of 1/20 C, aratio (ΔV₄/ΔV₃) of an absolute value (ΔV₄) of an amount of a potentialchanged per 10 mAh/g of the positive electrode immediately before thecompletion of full charging to an absolute value (ΔV₃) of an amount of apotential changed per 10 mAh/g of the negative electrode immediatelybefore the completion of full charging satisfies a relationshipΔV₄/ΔV₃>1.
 6. The secondary battery according to claim 1, wherein, inthe initial stage of using the secondary battery, excess conduction ionsare present in the positive electrode at the time of completing fullcharging.
 7. The secondary battery according to claim 6, wherein, in aperiod of time of the secondary battery being used, when the conductionions that contribute to charging and discharging decrease, the decreasedconduction ions are compensated for by the excess conduction ions in thepositive electrode.
 8. The secondary battery according to claim 1,wherein the secondary battery is a lithium ion secondary battery.
 9. Amethod for using a secondary battery including at least a positiveelectrode, a negative electrode, a separation layer that spatiallyseparates the positive electrode and the negative electrode, and an ionconductor that is held between the positive electrode and the negativeelectrode and has a function of conducting ions between the positiveelectrode and the negative electrode, wherein, in an initial stage ofusing the secondary battery, the secondary battery is used under acondition of a potential increase rate of the positive electrodeimmediately before completion of full charging being smaller than apotential decrease rate of the negative electrode immediately before thecompletion of full charging and is used under a condition of a potentialdecrease rate of the positive electrode immediately before completion offull discharging being smaller than a potential increase rate of thenegative electrode immediately before the completion of fulldischarging.
 10. The method for using a secondary battery according toclaim 9, wherein the secondary battery is continuously used until astate in which the potential increase rate of the positive electrodeimmediately before the completion of full charging becomes larger thanthe potential decrease rate of the negative electrode immediately beforethe completion of full charging.
 11. The method for using a secondarybattery according to claim 9, wherein, in the initial stage of using thesecondary battery, the secondary battery is used under a condition inwhich, when discharging is carried out with a constant current of 1/20C, a ratio (ΔV₂/ΔV₁) of an absolute value (ΔV₂) of an amount of apotential changed per 10 mAh/g of the positive electrode immediatelybefore the completion of full discharging to an absolute value (ΔV₁) ofan amount of a potential changed per 10 mAh/g of the negative electrodeimmediately before the completion of full discharging satisfies arelationship ΔV₂/ΔV₁<1.
 12. The method for using a secondary batteryaccording to claim 9, wherein, in the initial stage of using thesecondary battery, the secondary battery is used under a condition inwhich, when charging is carried out with a constant current of 1/20 C, aratio (ΔV₄/ΔV₃) of an absolute value (ΔV₄) of an amount of a potentialchanged per 10 mAh/g of the positive electrode immediately before thecompletion of full charging to an absolute value (ΔV₃) of an amount of apotential changed per 10 mAh/g of the negative electrode immediatelybefore the completion of full charging satisfies a relationshipΔV₄/ΔV₃<1.
 13. The method for using a secondary battery according toclaim 9, wherein the secondary battery is continuously used until astate in which, when charging is carried out with a constant current of1/20 C, a ratio (ΔV₄/ΔV₃) of an absolute value (ΔV₄) of an amount of apotential changed per 10 mAh/g of the positive electrode immediatelybefore the completion of full charging to an absolute value (ΔV₃) of anamount of a potential changed per 10 mAh/g of the negative electrodeimmediately before the completion of full charging satisfies arelationship ΔV₄/ΔV₃>1.
 14. The method for using a secondary batteryaccording to claim 9, wherein, in the initial stage of using thesecondary battery, excess conduction ions are present in the positiveelectrode at the time of completing full charging.
 15. The method forusing a secondary battery according to claim 14, wherein, in a period oftime of the secondary battery being used, when the conduction ions thatcontribute to charging and discharging decrease, the decreasedconduction ions are compensated for by the excess conduction ions in thepositive electrode.
 16. The method for using a secondary batteryaccording to claim 9, wherein the secondary battery is a lithium ionsecondary battery.